β3-adrenoreceptor agonists, agonist compositions and methods of using

ABSTRACT

The invention provides β 3 -adrenoreceptor agonists, pharmaceutical compositions comprising β 3 -adrenoreceptor agonist compounds, and methods of using such compounds for stimulating, regulating or modulating metabolism of fats in adipose tissue in animals.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.09/164,047, filed Sep. 30, 1998, now abandoned, which claims the benefitof U.S. Provisional Patent Application Ser. No. 60/061,152, filed Sep.30, 1997, which are incorporated herein by reference in their entirety.

BACKGROUND

1. Technical Field

The present invention relates to the field of β₃-Adrenoreceptor agonistsand to methods of their preparation, formulation and use to stimulate,regulate and modulate metabolism of fats in adipose tissues in animals,particularly humans and other mammals. More particularly, the presentinvention relates to the field of treating obesity and overweightconditions in animals, particularly humans and other mammals andassociated effects of conditions associated with obesity and overweight,including Type II diabetes mellitus (non-insulin dependent diabetes),insulin resistance, glucose intolerance, hypothyroidism, morbid obesity,and the like.

2. Prior Art

It was long thought that obesity was a consequence of self-indulgenceand undisciplined behavior. Obesity was seen as evidence of gluttony,through a lack of will or capacity for self-discipline. The overweighthave been disparaged, and thinness has been celebrated. Indeed, theperception of thinness as a major aspect of human beauty andattractiveness has become endemic in modern culture, and overweightconditions and obesity has increasingly grown to be an unacceptablecondition for social reasons.

Masked by these cultural icons are the hard medical facts: for manyindividuals, a tendency to overweight and even obesity are oftensymptoms of organic disease or disorders of the metabolism, associatedwith serious and even life-threatening conditions. In medical economicterms alone, the costs attributable to overweight and obesity arestaggeringly high.

A wide variety of approaches to the alleviation of obesity have ebbedand flowed though modern culture, ranging from a diverse collection ofdietary strategies, to drugs, to surgical interventions, to hypnosis.All have met with indifferent success at best. Some have proved to beoutright quackery. Others have proved to be effective only for theshort-term, with loss of effectiveness over time. Still others haveproved to be generally or at least partially successful so long as theregimen is sustained, but long term compliance is difficult to attainand in some cases has proved hazardous to other aspects of health andwell-being. Some surgical procedures have had some successes, but aswith any invasive procedures, there are risks. Some approaches to weightloss and control, in the extreme, lead to conditions which arethemselves pathological, such as bulimia and anorexia nervosa. Othereffects are less extreme, but still highly undesirable, such asamennorhea, vitamin and essential nutrient deficiencies, and the like.

A great deal of the difficulty in the art and practice of obesity andoverweight management has been a consequence of attention focused on thecontrol of appetite, and reducing the amount of food intake. It has longbeen the belief of many that only by the control of caloric intake is itpossible to regulate body weight and fat deposition and utilization.Since appetite is controlled and regulated in the brain, brainpharmacology and the alteration of brain chemistry has been a primaryfocus of weight regulation and control efforts. Such approaches have ledto addictions to appetite suppressants, to primary pulmonary myopathy,cardiac valve damage, and to reports of serotonin disruptions anddisorders and psychotic episodes among users. Morbities and mortalitieshave been unacceptably high.

In another aspect of technology relating to fat is the dietary emphasison limiting dietary fat intake. For those who eat meats, there isincreasing emphasis on low fat content meats in the carcasses of theanimals employed in food stocks. Much recent efforts have been devotedto the production of beef, pork, poultry and the like with reduced fatcontent. Breeding patterns are being manipulated and generic engineeringof farm animals is being directed at lowering fat content of theanimals. The techniques of fattening of animals intended for table meatproduction is highly developed, but is gradually being limited by theemphasis on limiting dietary fats and interest in leaner carcassanimals.

Only in very recent times has obesity been addressed in relation to themetabolic pathways of the body and their role and import in fat storageand usage in the body.

Recent research has elucidated some of the mechanisms of obesity andoverweight, and has revealed that much of the limitation of prior andcurrent weight-loss techniques stems from the fact that they arebiochemically and particularly metabolically unsound and incapable ofstimulating, regulating and modulating metabolism of fats in adiposetissues. Without these characteristics, it is now known, weight loss andcontrol strategies are likely to fail or to produce conditions as bad asor worse than the weight problems they are intended to alleviate.Without heroic dedication and discipline, and even fanaticism, by thesubject, most strategies are short term in their weight loss and controleffects.

Increasing efforts have been directed to biochemical research into themechanisms of fat deposition and metabolism and into stimulating,regulating and modulating metabolism of fats in adipose tissues.Considerable recent progress has been made.

Among the biochemical work of note has been the recent recognition of arole of β-Adreno-receptor activity in the metabolism of fats. It hasbeen recognized that agonists for β-Adrenoreceptors have, in some cases,produced marked weight loss in animals, particularly humans and othermammals.

More recently, the loss of weight has been identified with theβ-Adrenoreceptor sub-type, β₃-Adrenoreceptors. The specific structure ofthe b3-Adrenoreceptor has been characterized, and demonstrated to be adistinct cellular structure which is Distinguishable from theb1-Adrenoreceptor and the b2-Adrenoreceptor.

It has been demonstrated that compounds which are significantβ₃-Adrenoreceptor agonists produce marked weight loss in animals, andthat the loss is sustained with continuation of the administration ofsuch compounds. These compounds provide potent regulation of fatmetabolism. The compounds employed to date are also agonists for theβ₁-Adrenoreceptor and the β₂-Adrenoreceptor sites. The lack ofselectivity represents unwanted side effects of such compounds, and thecompounds known as β₃-Adrenoreceptor agonists to date are not suitablecandidates for therapeutic usage because of the unwanted and dangerousside effects.

PROBLEMS AND NEEDS IN THE ART

The existing strategies for weight and body fat regulation areinadequate. The current strategies are ineffective, unsafe, or both.Whether through diet manipulations or through drug usage, orcombinations of such strategies, there is a lack of a clear path to safeand effective regulation of body weight and body fat which is safe andeffective, which can provide significant and long lasting relief fromthe health consequences of overweight and obesity and the conditionsassociated therewith, and from the disease conditions which areaggravated by overweight and obesity.

It is clear that the art lacks and needs therapeutic agents which arehighly potent and highly selective β₃-Adrenoreceptor agonists foreffective stimulation, regulation and modulation of metabolism of fatsin adipose tissues.

It is also clear that the art lacks and needs agents which are effectiveβ₃-Adrenoreceptor agonists free of unwanted side effects, and which aresafe for stimulating, regulating and modulating metabolism of fats inadipose tissues.

It is clear that the art lacks and needs agents which are effective atregulating the body fat of animals, particularly humans and othermammals, both in the reduction of body weight in the obese and theattendant health problems and issues, and in the production of low fattable meats from domesticated animals for human consumption.

OBJECTS OF THE INVENTION

It is an object of the present invention to provide novel compoundswhich are safe and effective β₃-Adrenoreceptor agonists.

It is another object of the present invention to provide syntheses ofsuch β₃-Adrenoreceptor agonists.

Another object of the present invention is the provision of safe andeffective β₃-Adrenoreceptor formulations for administration tostimulate, regulate and modulate metabolism of fats in adipose tissuesin animals, particularly humans and other mammals.

Still another object of the present invention is to provide safe andeffective administration of β₃-Adrenoreceptor agonists for stimulating,regulating and modulating metabolism of fats in adipose tissues inanimals, particularly humans and other mammals.

Yet another object of the present invention is to provide a safe andeffective regimen for causing and promoting weight loss in humans, andfor the maintenance of healthy and personally desired body fat levels.

Still another object of the present invention is to provide safe andeffective adjuncts to the husbandry of domesticated animals for theproduction of low fat dietary meats for human consumption.

The primary objective of the present invention is to provide for weightand body fat regulation through modalities which are effective and safe.The present invention provides a clear path to safe and effectiveregulation of body weight and body fat which is safe and effective,which can provide significant and long lasting relief from the healthconsequences of overweight and obesity and the conditions associatedtherewith, and from the disease conditions which are aggravated byoverweight and obesity.

These and related objectives are met by the terms of the presentinvention as set out in detail in the following specification anddefined in the claims appended hereto.

SUMMARY OF THE INVENTION

Compounds which are highly potent and highly specific β₃-Adrenoreceptoragonists are provided. The compounds are formulated into pharmaceuticalpreparations and administered for stimulating, regulating and modulatingmetabolism of fats in adipose tissues in animals, particularly humansand other mammals.

The compounds of the invention have one of the structures:

wherein:

R₁ and R₃ are independently members selected from the group consistingof H, F, Cl, Br, I, OCH₃, CF₃, CH₃, alkyl and aryl alkyl;

R₂ is a member selected from the group consisting of H, I, OCH₃, NH₂,NHR₁₃, NHCOR₁₃, NHCONHR₁₃ and NHCOSR₁₃, and provided that, when both R₁and R₃ are CF₃, R₂ is not H;

R₄ and R₅ are each members independently selected from the groupconsisting of H, OH, F, Cl, Br and I, and provided that, when R₄ and R₅are both OH or both OCH₃, then R₂ is neither NH₂ nor OCH₃;

R₆ and R₇ are independently members selected from the group consistingof H, F, Cl, Br and I;

R₈ and R₁₃ are independently members selected from the group consistingof H, lower alkyl and aryl alkyl of from 1 to about 8 carbons, F, Cl,Br, I, OCH₃, and CF₃, and provided that, when R₁₃ is CH₃, only one ornone of R₁ and R₃ is I;

wherein R₉ and R₁₀ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁, and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and wherein R₁ and R₂, taken together, R₂ and R₃, taken together and R₄and R₅, taken together may additionally form a member selected from thegroup consisting of moieties having the structure:

wherein R₁₃ and R₁₄ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁ and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and the simple inorganic and lower alkyl, of from 1 to about 8 carbons,carboxyllic acid salts thereof.

The preferred compounds of the invention are those wherein one of R₄ andR₅ is OH and the other is H. More preferably, R₅ is OH and R₄ is H. Mostpreferably, the compound has the following structure:

The invention is also directed to a method and pharmaceuticalcomposition for stimulating, regulating and modulating metabolism offats in adipose tissues in animals comprising preparing andadministering an effective amount of a β₃-Adrenoreceptor selectiveagonist which is a member of the group consisting of:

wherein:

R₁ and R₃ are independently members selected from the group consistingof H, F, Cl, Br, I, OCH₃, CF₃, CH₃, alkyl and aryl alkyl;

R₂ is a member selected from the group consisting of H, I, OCH₃, NH₂,NHR₁₃, NHCOR₁₃, NHCONHR₁₃ and NHCOSR₁₃;

R₄ and R₅ are each members independently selected from the groupconsisting of H, OH, F, Cl, Br and I;

R₆ and R₇ are independently members selected from the group consistingof H, F, Cl, Br and I;

R₈ and R₁₃ are independently members selected from the group consistingof H, lower alkyl and aryl alkyl of from 1 to about 8 carbons, F, Cl,Br, I, OCH₃, and CF₃;

wherein R₉ and R₁₀ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁ and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and wherein R₁ and R₂, taken together, R₂ and R₃, taken together and R₄and R₅, taken together may additionally form a member selected from thegroup consisting of moieties having the structure:

wherein R₁₃ and R₁₄ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁ and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and the simple inorganic and lower alkyl, of from 1 to about 8 carbons,carboxyllic acid salts thereof.

Preferably, the method and composition use an agonist wherein one of R₄and R₅ is OH and the other is H. More preferably, R₅ is OH and R₄ is H.Most preferably, the agonist has the following structure:

These compounds are formulated into pharmaceutical carriers to serve ashighly selective, effective and safe β₃-Adrenoreceptor agonists toprovide long term weight control.

In humans, the compositions are administered to control body fat levels,and to maintain acceptable body fat levels over time.

In domesticated animals, the compositions are administered to attaindesirably low fat content in carcass meats intended for humanconsumption.

DETAILED DESCRIPTION

The following is a description of the invention, the compounds of thepresent invention, the method of their synthesis, their formulation intopharmaceutical compositions suitable for administration, and the methodof their use for stimulating, regulating and modulating metabolism offats in adipose tissues in animals, particularly humans and othermammals.

The discussion and presentation of bioactivity information and data inthe present description is made in compliance with the standards of theJournal of Medicinal Chemistry. All chemical compounds are named inaccordance with the standards of the American Chemical Society rules ofstandard nomenclature, employing accepted “trivial names” whereapplicable. All chemical structures are shown in “skeletal” form, forclarity in understanding the most significant considerations andinformation about the structures, with implicit hydrogen atoms notrelevant to the conformation of structures not shown, in the fashiontypically employed in the Journal of Medicinal Chemistry and most otherjournals of chemistry. The use of such structural notation is mostconvenient to understand the structures of such molecules, and those ofordinary levels of skill in the relevant arts are accustomed to suchrepresentations and are readily able to identify and understand such“skeletal” structures, including the implicit hydrogen atoms not shown.

Introduction

The risks and unacceptable levels of adverse consequences of many weightcontrol and weight loss strategies available to individuals and to themedical community make the development of safe and effective modalitiesfor stimulating, regulating and modulating metabolism of fats in adiposetissues an important need in the art and in society as a whole.

The importance of regulating dietary fat intake, and particularlysaturated animal fat, has long been recognized. Consumption of meats isprimary in the diet in most developed countries, and substantial effortshave been devoted to the development of leaner animals, among otherstrategies, to facilitate regulating and limiting of dietary intake ofsaturated animal fats.

In the present invention, the highly desirable goals of stimulating,regulating and modulating metabolism of fats in adipose tissues inanimals, particularly humans and other mammals through the modality ofadministering a pharmaceutical formulation of one or more compoundswhich are β₃-Adrenoreceptor selective agonists is provided.

The regulatory and modulatory effect of the compounds of the presentinvention are dependent on continued administration over time, and theattainment of an equilibrium state which is believed to be dosedependent. In that fashion, the present invention affords the control ofbody fat in animals, particularly humans and other mammals, oversustained periods, at desirable levels of body fat and/or body massindices, as defined in the medical literature.

Overview of the Invention

Safe and effective control of body fat and body mass indices have been along sought but quite elusive goal for the medical community. Themodalities in use over the past half century have proved to be bothdangerous and limited in effectiveness. The longer the effort issustained, in general, the higher the risk and the lower theeffectiveness.

The weight loss effect of β-Adrenoreceptor agonists generally has beenknown per se for a considerable period. That recognition has not led tosafe and effective weight loss or regulation because of the copious andhighly dangerous side effects.

The recent discovery of the β₃-Adrenoreceptor and its focal role in fatmetabolism holds the promise of the employment of β₃-Adrenoreceptoragonists in weight loss and regulation. Through the development ofcompounds which are highly selective for the β₃-Adrenoreceptor withoutactivation of the β₁ Adrenoreceptor and β₂ Adrenoreceptor the presentinvention makes that goal attainable.

The β₃-Adrenoreceptor has not been characterized to date, which makesthe search for safe and effective agonists with the required highselectivity a difficult and arduous task. Without a clear understandingof the receptor binding site, the design of effective compounds is basedlargely on structural activity correlations which are uncertain,unpredictable and unreliable. Even the most minor changes in structurecan produce wide deviations in binding affinity, binding specificity,and agonist activity. The compounds of the present invention attain thehigh affinity for the β₃-Adrenoreceptor, the low affinity for the β₁Adrenoreceptor and the β₂ Adrenoreceptor required for effectiveselectivity and freedom from adverse side effects, and high levels ofagonist activity to make the compounds effect in their required role infat metabolism.

The β-Adrenoreceptor Family

β Adrenoreceptors have long been known and have been studied for theirrole in response to the catechol amine hormones adrenaline(epinephrine), noradrenaline (norepinephrine) and dopamine.

Adrenaline, to exemplify the biochemical action of these catechol aminehormones, is a primary agonist for these receptors in the body, andactivates metabolic processes within the cells to which it binds.Adrenaline is associated with specific cellular processes which aredependent upon the nature of the cell to which it is bound. The actionof adrenaline on the cell is to activate an enzyme within the cell,adenylate cyclase. The adenylate cyclase in turn catalyses furtherreactions within the target cell, typically beginning an enzyme cascadeuntil the enzyme is broken down or deactivated by cellular regulatorymechanisms. The primary action of adenylate cyclase is the conversion ofATP to cAMP (cyclic adenosine monophosphate or “cyclic adenylate”).

In the liver cells, the cAMP activates, in turn, an enzyme cascade whichcatalyses the conversion of glycogen into glucose and inhibits theconversion of glucose into glycogen, greatly increasing extra-cellularlevels of blood glucose in the body.

In muscle tissues, cAMP triggers the breakdown of glycogen into lactateand ATP, providing high levels of ATP to support high levels of muscularactivity. In the heart muscle, in particular, the effect is hypertensiveand is accompanied by vasodilation throughout the body, increasing bloodflow and transport of blood glucose to the cells.

β-blockers are among the commonly prescribed drugs in the field ofcardiology. For the hypertensive patient, competitive binding of theblocking agent to the β Adrenoreceptors modulates and limits theadditional hypertensive action of adrenaline on the heart muscle. Theβ-blockers may be employed in combination with vasodilators, decreasingthe resistance to blood flow peripherally without increasing the heartrate and strength of contraction. A reduction in blood pressure and thework requirement on the heart muscle results.

In the lung, cAMP acts to cause bronchodilation which, when combinedwith increased blood flow, supplies higher levels of oxygen transport.

(Adrenaline, or epinephrine, is widely employed to stimulatebronchodilation in the treatment of asthma and allergenic reactionswhich constrict the bronchia.)

Others of the catechol amine hormones have comparable activities.

The release of free fatty acids from adipose tissue has been observed asan action provided by β Adrenoreceptor agonists.

A variety of β Adrenoreceptor agonists and blockers have been known forsome time, and have proved to be a fruitful field for drug development.

It has been recognized that there are sub-types of the β Adrenoreceptor,designate the β₁ Adrenoreceptor and the β₂ Adrenoreceptor. Lands, etal., “Differentiation of Receptor Systems Activated by SympathomimeticAmines” Nature, 214:597-598 (1967). Lands, et al, associate the releaseof free fatty acids from adipose tissue with β₁ Adrenoreceptoractivation.

Subsequent studies have provided a spectrum of β Adrenoreceptor agonistsand blockers. Among the blockers are both competitive andnon-competitive (non-equilibrium) binding agents. Some of such agentsare ubiquitous in their action, while others exhibit varying degrees ofselectivity for the two sub-types (and hence in the action responseproduced).

Selective agonist studies show both qualitative and quantitativedifferentiation of the sub-types. β₁ Adrenoreceptor activation have beendemonstrated to cause cardiac stimulation, release of free fatty acidsfrom adipose tissue, and intestinal inhibition. In contrast, β₂Adrenoreceptor activation produces broncho- and vaso-dilation.

The β₃-Adrenoreceptor

Quite recently, a third sub-type of the β Adrenoreceptor family has beenidentified. Howe, R. “Beta-3 adrenergic agonists.” Drugs Future 1993,18, 529-549. It has been designated the β3 Adrenoreceptor. It has alsobeen specifically identified with the release of free fatty acids fromadipose tissue, previously attributed by Lands et al. with the β1Adrenoreceptor.

While β₁ Adrenoreceptor and β₂ Adrenoreceptor sites are ubiquitous, ithas been found that the β₃-Adrenoreceptor sites are more specialized andare predominantly located on adipose tissue cells, and from studies todate appear to be rather specifically associated with the metabolism offats.

β₃-Adrenoreceptor Agonists

This discovery leads quite directly to the search for selective andpotent agonists for the β₃ Adrenoreceptor for the treatment of obesityand control of weight. The search is hindered by the lack ofcharacterization of the receptor, but the information from bindingstudies and other work on β Adrenoreceptor agonists generally indicatesthat β₃ Adrenoreceptor agonists should be similar in structure to thecatechol amine hormones.

Rather little has been published to date on β₃ Adrenoreceptor agonists.See, however, Howe, R. “Beta-3 adrenergic agonists” Drugs Future 1993,18, 529-549. It is accordingly necessary to extrapolate from theinformation available about β₁ Adrenoreceptor and β₂ Adrenoreceptoragonists, and to engage in an attempt to discern structural and activityrelationships from the available data. The following comments on β₁Adrenoreceptor and β₂ Adrenoreceptor considerations summarizes what isknown in the literature upon which the effort to developβ₃-Adrenoreceptor agonists can be based.

Trimetoquinol is a potent nonspecific β-adrenoreceptor (β-AR) agonistclinically used in Japan as a bronchorelaxant. Iwasawa, Y.; Kiyomoto, A.“Studies of tetrahydroisoquinolines (THI) 1. Bronchodilator activity andstructure-activity relationships.” Jap. J. Pharmacol. 1967, 17, 143-152.Optical resolution of trimetoquinol and subsequent evaluation of thestereoisomers revealed that the (S)-(−)-isomer of trimetoquinol is apotent β-adrenoreceptor agonist in heart and lung tissues; whereas, the(R)-(+)-isomer acts as a selective and highly stereospecific thromboxaneA₂/prostaglandin H₂ (TP) receptor antagonist. Yamamoto, E.; Hirakura,M.; Sugasawa, S. “Synthesis of6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline derivatives” TetraheronSuppl. 1966, 8 (Part 1), 129-134. Mayo, J. R.; Navaran, S. S.; Akbar,H.; Miller, D. D.; Feller, D. R. “Stereodependent inhibition of humanplatelet function by the optical isomers of trimethoquinol” Biochem.Pharmacol. 1981, 30, 2237-2241. Ahn, C. H.; Romstedt, K. J.; Wallace, L.J.; Miller, D. D.; Feller, D. R. “Characterization of the inhibition ofU46619-mediated human platelet activation by the trimetoquinol isomers.Evidence for endoperoxide/thromboxane A₂ receptor blockade” BiochemPharmacol 1988, 37, 3023-33. Shin, Y.; Romstedt, K. J.; Miller, D. D.;Feller, D. R. “Stereodependent antagonism of thromboxaneA₂/prostaglandin H₂ receptor sites by trimetoquinol isomers in humanplatelets, rat vascular endothelial cells and rat vascular smooth musclecells” Pharmacol. Commun. 1993, 1, 303-312. Radioligand competitionbinding studies at β-adrenoreceptor and TP receptors show highstereoselective binding (>100-fold) for the S(−)-isomer and R(+)-isomer,respectively. This stereoselectivity is also observed in the binding offluorinated trimetoquinol analogs at β-adrenoreceptor. Clark, M. T.;Adejare, A.; Shams, G.; Feller, D. R.; Miller, D. D. “5-fluoro- and8-fluorotrimetoquinol: selective beta 2-adrenoceptor agonists” J MedChem 1987, 30, 86-90.

The basic catechol structure of catecholamine hormones, such asepinephrine, norepinephrine, dopamine, and the β-adrenoreceptor agonistisoproterenol, is incorporated within the tetrahydroisoquinoline nucleusof trimetoquinol. In studies using mutated hamster β₂ Adrenoreceptorexpressed in Chinese hamster ovary (CHO) cells, replacement of Asp113with Asn113 abolished receptor binding of trimetoquinol and its analogs.Fraundorfer, P. F. “Functional and biochemical characterization oftrimetoquinol (TMQ) analog interactions with β-adrenergic receptorsubtypes” Ph. D. Thesis, The Ohio State University, 1993(“Fraundorfer-2”). In addition, replacement of Ser204 and Ser207 withAla204 and Ala207 decreased the binding affinity of trimetoquinolanalogs in β₂ Adrenoreceptor to a lesser extent, but greatly diminishedtheir ability to stimulate cAMP accumulation. “Fraundorfer-2”, supra.However, both the binding and functional activities of isoproterenol aresignificantly reduced in the β₂ adrenoreceptor Asn113, Ala204 and Ala207mutants. These results suggest that although trimetoquinol analogs mayinteract with the same amino acid residues in the binding site asisoproterenol, the contribution of catechol interactions with thesemutated β₂ Adrenoreceptors is less significant in terms of ligandbinding and may well be overshadowed by the binding contributions of thetrimethoxybenzyl group of trimetoquinol.

Substitution with fluorine or iodine on the 5- or 8-positions oftrimetoquinol resulted in only a modest (˜10-fold) increase in β₂Adrenoreceptor versus β₁ adrenoreceptor selectivity as compared totrimetoquinol in functional and binding studies. Clark, et al., supra;Fraundorfer, P. F.; Fertel, R. H.; Miller, D. D.; Feller, D. R.“Biochemical and pharmacological characterization of high-affinitytrimetoquinol analogs on guinea pig and human beta adrenergic receptorsubtypes: evidence for partial agonism” J Pharmacol Exp Ther 1994, 270,665-74. In addition, it has also found that replacement of the 3′- and5′-methoxy substituent of trimetoquinol with iodine atoms (i.e., 2) iswell tolerated on both β-adrenoceptor, Fraundorfer, et al., supra, andTP receptors. Shin, Y.; Romstedt, K. J.; Miller, D. D.; Feller, D. R.“Interactions of nonprostanoid trimetoquinol analogs with thromboxaneA₂/prostaglandin H₂ receptors in human platelets, rat vascularendothelial cells and rat vascular smooth muscle cells” J Pharmacol ExpTher 1993, 267, 1017-23.; Harrold, M. W.; Gerhardt, M. A.; Romstedt, K.;Feller, D. R.; Miller, D. D. “Synthesis and platelet antiaggregatoryactivity of trimetoquinol analogs as endoperoxide/thromboxane A2antagonists” Drug Des Deliv 1987, 1, 193-207.

Interestingly, although its binding affinity at β₁ adrenoreceptor isslightly better than trimetoquinol, compound 2 displays a much higheraffinity than trimetoquinol for β₂ adrenoreceptor:

These earlier findings suggest that trimetoquinol analogs interact withan auxiliary site through the substituted benzyl group in addition tothe binding site shared by catecholamines. This subsite can be used toadvantage in the development of more site-selective agents. The highpotency of compound 2 seems to suggest that this auxiliary site ishydrophobic in nature. On TP receptors, the complementary binding sitesfor trimetoquinol analogs are essentially unknown. However, compound 2is a more potent TP receptor antagonist than trimetoquinol furthersuggesting that 1-benzyl ring modifications are appropriate to developagents with greater selectivity on β-adrenoreceptor versus TP receptorsand vice versa.

The literature describes the synthesis and evaluation of iodinatedtrimetoquinol analogs designed as probes for characterizing the receptorbinding interactions, associated with the benzyl substituent oftrimetoquinol analogs and as site-selective β-adrenoreceptor and TPreceptor ligands. These chemical modifications provide a greaterseparation of the pharmacological activities for this class ofcompounds. Site-selective β-adrenoreceptor agents have potential in thetreatment of cardiopulmonary diseases, non-insulin dependent diabetes(Type II) and obesity, Howe, R., “Beta-3 adrenergic agonists” DrugsFuture 1993, 18, 529-549, whereas highly selective TP receptorantagonists have value in the treatment of thrombolytic disorders. Shin,supra; Shin, Y.; Romstedt, K. J.; Miller, D. D.; Feller, D. R.,“Interactions of nonprostanoid trimetoquinol analogs with thromboxaneA₂/prostaglandin H₂ receptors in human platelets, rat vascularendothelial cells and rat vascular smooth muscle cells” J Pharmacol ExpTher 1993, 267, 1017-23; Shin, Y.; Romstedt, K.; Doyle, K.; Harrold, M.;Gerhardt, M.; Miller, D.; Feller, D., “Pharmacologic antagonism ofthromboxane A₂ receptors by trimetoquinol analogs.” Chirality 1991, 3,112-117.

Other known β₁-adrenoreceptor and β₂-adrenoreceptor agonists includeisoproterenol, X and Y, having the structures:

While these compounds are highly active β₃-adrenoreceptor agonists, theyare also non-selective, and also bind and activate the β₁-adrenoreceptorand β₂-adrenoreceptor with comparable affinities and activities. Theyare thus entirely unsuited for use in the present invention, but they doafford good basis for comparative and competitive binding studies, andare employed in the present invention for those purposes whenappropriate.

The Compounds of the Invention

The present invention is based on the provision of β₃-adrenoreceptoragonists in pharmaceutically acceptable carrier formulations foradministration to stimulate, regulate and modulate metabolism of fats inadipose tissues in animals, particularly humans and other mammals.

The present invention additionally provides a method for safe andeffective administration of β₃-Adrenoreceptor agonists for stimulating,regulating and modulating metabolism of fats in adipose tissues inanimals, particularly humans and other mammals.

The present invention provides potent, highly selectiveβ₃-Adrenoreceptor agonists which are compounds having the structures:

wherein:

R₁ and R₃ are independently members selected from the group consistingof H, F, Cl, Br, I, OCH₃, CF₃ and CH₃, alkyl and aryl alkyl;

R₂ is a member selected from the group consisting of H, I, OCH₃, NH₂,NHR₈, NHCOR₁₃, NHCONHR₁₃ and NHCOSR₁₃, and provided that, when both R₁and R₃ are CF₃, R₂ is not H;

R₄ and R₅ are each members independently selected from the groupconsisting of H, OH, F, Cl, Br and I, and provided that, when both R₄and R₅ are OH, then R₂ is neither NH₂ nor OCH₃;

R₆ and R₇ are independently members selected from the group consistingof H, F, Cl, Br and I;

R₈ and R₁₃ are independently members selected from the group consistingof H, lower alkyl of from 1 to about 8 carbons, F, Cl, Br, I, OCH₃, andCF₃

wherein R_(9 and R) ₁₀ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁ and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and wherein R₁ and R₂, taken together, R₂ and R₃, taken together and R₄and R₅, taken together may additionally form a member selected from thegroup consisting of moieties having the structure:

wherein R₁₃ and R₁₄ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and where R₁₁ and R₁₂ are independently members selected from the groupconsisting of H, lower straight chain and branched alkyl of from 1 to 8carbon atoms,

and the simple inorganic and lower alkyl, of from 1 to about 8 carbons,carboxyllic acid salts thereof.

It is preferred that the compounds of the present invention be furtherqualified and limited to those with high selectivity and high activityfor the β₃-Adrenoreceptor

In addition, there are several particularly preferred species, i.e.,specific compounds, which are preferred. These particularly preferredspecies include the following compounds:

Of these compounds, the following are preferred, A1, A2, A3, A4, A5, A6,A7, A8, A9, A10, A20, A21, A22, A23, A24, A25, A26, A27, A30, A31, A32,A33, A34, A36, A37, A38, A41, A42, A44, A45, A46, and all of the Bcompounds. At present, the most preferred compound is A4.

Synthesis of TMQ Derivatives

A convenient protection scheme has been devised for the synthesis of thedesired β₃-Adrenoreceptor agonists of the present invention. The tripleprotected isoquinoline intermediates were synthesized as shown inScheme 1. The tetrahydroisoquinolines 6a-c were synthesized from theO-methyl or O-benzyl protected catecholamines 3a or 3b, respectively,and 4-nitrophenylacetic acid (4a) or 3,5-bis-trifluoromethylphenylaceticacid (4b) using methods described previously. Clark, M. T.; Adejare, A.;Shams, G.; Feller, D. R.; Miller, D. D. “5-fluoro- and8-fluorotrimetoquinol: selective beta 2-adrenoceptor agonists” J MedChem 1987, 30, 86-90.; Harrold, M. W.; Gerhardt, M. A.; Romstedt, K.;Feller, D. R.; Miller, D. D. “Synthesis and platelet antiaggregatoryactivity of trimetoquinol analogs as endoperoxide/thromboxane A2antagonists” Drug Des Deliv 1987, 1, 193-207. Adejare, A.; Miller, D.D.; Fedyna, J. S.; Ahn, C. H.; Feller, D. R. “Syntheses andbeta-adrenergic agonist and antiaggregatory properties of N-substitutedtrimetoquinol analogues” J Med Chem 1986, 29, 1603-9. The amino group of6a and 6b were protected with trifluoroacetyl (TFA) andt-butyloxycarbonyl (t-BOC), respectively. The nitro groups of 7a,b werereduced via catalytic hydrogenation using Pd/C or Raney Nickel,respectively, to give the aniline derivatives 8a,b. Iodination of 8a,bwith 1 equivalent of benzyltrimethylammonium dichloroiodate (BTMACl₂I)according to Kajigaeshi et al., Kajigaeshi, S.; Kakinami, H.; Fujisaki,S.; Okamoto, T. “Halogenation using quaternary ammonium polyhalides.VII. Iodination of aromatic amines by use of benzyltrimethylammoniumdichloroiodate (I⁻)” Bull. Chem. Soc. Jpn. 1968, 61, 600-602, led to the3′-iodo analogs 9a,b. An additional 3 equivalents of BTMACl₂I added inportions over a 3 day period was required to convert 8a completely tothe diiodo derivative 10a.

While reaction of 10a with acetic anhydride at room temperature did notgive the desired 4′-acetamido derivative 13, heating 10a in aceticanhydride at reflux resulted in the diacetylation product 16(Scheme 3).Similar diacetylation has been reported with the reaction of2,6-dibromo-4-toluidine with refluxing acetic anhydride while lowertemperatures gave a mixture of mono and diacetylated products. Ulffers,F.; von Janson, A. Diacetylderivate einger Amine der aromatischen ReiheBer. 1894, 27, 93-101. With this in mind, mono-acetylation wasaccomplished by reacting 10a with 5 equivalents of acetyl chloride inthe presence of 4-dimethylaminopyridine (DMAP) and triethylamine at roomtemperature to afford 13. Basic hydrolysis of the trifluoroacetylprotecting group of 10a and 13gave 20c and 14, respectively. The methoxyderivatives 20c, 14, and 6c were demethylated with BBr₃ to afford thedesired trimetoquinol analogs 21c, 15, and 27, respectively, ashydrobromide salts (Sch m 1 and 3). In a similar manner, the6,7-dibenzyloxy-1-(3,5-diiodo-4-methoxybenzyl)-1,2,3,4-tetrahydro-isoquinoline,Harrold, M. W.; Gerhardt,. M. A.; Romstedt, K.; Feller, D. R.; Miller,D. D. Synthesis and platelet antiaggregatory activity of trimetoquinolanalogs as endoperoxide/thromboxane A2 antagonists Drug Des Deliv 1987,1, 193-207, was dealkylated with BBr₃ to give6,7-dihydroxy-1-(3,5-diiodo-4-hydroxybenzyl)-1,2,3,4-tetrahydroisoquinoline(18) the desmethyl analog of 2. Diazotization of 10a (Scheme 3) followedby reaction of the diazonium salt with H₃PO₂ or potassium iodide (KI)gave the diiodo and triiodo derivatives, 19a and 19b, respectively.Basic hydrolysis of the trifluoroacetyl group of 19a,b as before gave20a,b. Demethylation of 20a,b with BBr₃ proceeded smoothly to give21a,b. Compound 9a was acylated with acetic anhydride in refluxingbenzene to give 22which was deprotected in the same manner as 14to give23(Scheme 4).

However, attempts to demethylate 23with BBr₃ failed to give the desiredproduct 26a. Surprisingly, the amide bond of 23was cleaved to giveaniline 24. This indicates the importance of both ortho-iodine atoms asa stenc hindrance toward cleavage of the acetamido group of 14by BBr₃.Trimethylsilyliodide (TMSI) was thus employed as a mild reagent forether cleavage. However, this agent was too weak to effect demethylationof 23; therefore, the catechol O-methyl ether protecting groups werechanged to benzyl ethers. Hence, compounds 26a and 26b were preparedfrom the O-benzyl and N-t-BOC protected 9b (Schem 4). The acylatedcompounds 25a and 25b were deblocked using TMSI. Initially, using theprocedure of Lott, R. S.; Chauhan, V. S.; Stammer, C. H. “Trimethylsilyliodide as a peptide deblocking agent” J. Chem. Soc. Chem. Comm. 1979,495-496, (TMSI, MeCN, 50° C. 2 h) amide 25a gave the desired amide 26aalong with a significant amount of the deacetylation product 24.Ordinarily, amides are stable to TMSI. To optimize the selectivity, theTMSI deprotection reaction was monitored by NMR spectroscopy at roomtemperature. The O-benzyl protecting groups were removed within 6 h andno cleavage of the amide bond was observed at this temperature for 20 h.Thus, using the following reaction conditions: 4-6 eq. of TMSI, MeCN,room temperature, 6 h, 26a and 26b from 25a and 25b were obtained,respectively.

The proton NMR spectra of synthesized compounds were quite complicated,especially the 2-t-BOC derivatives which displayed complex splittingpatterns reflecting two relatively stable conformations with ratiosranging from 5:2 to 5:4, similar to those observed for N-Ac and N-Mesubstituted tetrahydroisoquinolines,. Dalton, D. R.; Cava, M. P.; Buck,K. T. “Hindered rotation in1-benzyl-1,2,3,4-tetrahydro-6,7-dimethoxyisoquinolines” Tett. Lett.1965, 2687-2690; Tomita, M.; Shingu, T.; Fujitani, K.; Furikawa, H.“Studies on the alkaloids of menispermaceous plants. CCXVI. Nuclearmagnetic resonance spectra of benzylisoquinoline derivatives. (1).N-Methylcoclaurine type bases” Chem. Phar. Bull. 1965, 13, 921-926.However, the ¹³C NMR spectra of 1-benzyl tetrahydroisoquinolines can beeasily used for structure identification because of their relativesimplicity. Assignments of signals (final compounds) were made based onthe ¹³C-NMR spectra of salsolinol, Iwasa, K.; Kamigauchi, M.; Takao, N.“Metabolism of salsalinol by tissue cultures of some Papaveraceae”Phytochemistry 1991, 30, 2973-2975, on effects of substituents inbenzene ring, and off-resonance spectra. For 2-TFA derivatives, thechemical shift of the C-3 atom appears as a quartet (⁴J C-F≈3.7 Hz)indicating its close proximity to the CF₃ group.

It should be noted that all the compounds produced in the foregoingsyntheses are racemic mixtures of the stereoisomers, with a site ofasymmetry at C₁₀. It has been observed that the binding specificity andactivity of the individual isomers will differ, with the (−) speciesgenerally the more specific and active as agonists. Typically, thedifference will be relatively modest, and the values of the (+/−)racemic mixtures will be intermediate of the values of the individualisomers and are generally equivalent in their bioactivities to theisolated isomers. It is generally preferred to employ the racemicmixture for reasons of economy and simplicity of the synthesis, but theindividual isomers are also a part of the present invention In suitablecases, the individual isomers can be isolated by stereospecificsynthesis or by separatory techniques, both of which are per se known tothose of ordinary levels of skill in the art.

Little has been published on the biochemical action of β₃-adrenoreceptoragonists and the behavior of these compounds in vivo is not entirelyclear. What is clear is that the activity of these agents is dependentupon binding to the β₃-adrenoreceptor. It is also clear that affinityalone is not the sole consideration, as the compounds vary in theirselectivity, some also binding β₁ adrenoreceptor and β₂ adrenoreceptorsites, producing unwanted side effects consistent with a role asagonists or blockers of those sites. They also vary in the degree ofagonist activity when bound at the β₃-adrenoreceptor agonists site. Theeffect is at least analogous to adrenaline binding to theβ₃-adrenoreceptor and the agonist activity provided by adrenaline, butin the present invention is more selective and substantially free of β₁adrenoreceptor agonist or blocker activity, β₂ adrenoreceptor agonist orblocker activity, or TP agonist or blocker activity.

The mode of action of these agonists when bound at the β₃-adrenoreceptorsite has not been fully characterized. Although there is no wish to bebound thereby, it is believed that the activation of the cellularmechanisms produced by the agonist activity is the same as that providedby adrenaline, which has been studied. No indications have been seenwhich are inconsistent with the adrenaline-like agonist behavior, exceptthat the compounds of the present invention are far more selective forthe β₃-adrenoreceptors and minimally bound to the β₁ adrenoreceptor andβ₂ adrenoreceptor sites.

The action of the β₃-adrenoreceptor agonists of the present inventionare also more persistent than the effect of adrenaline. The compoundsappear to be less readily broken down in vivo, remain bound to theβ₃-adrenoreceptor sites longer than does adrenaline, and continue to beactive for a longer prior of time. It is known that the effects ofadrenaline are very rapidly induced by the release of adrenaline intothe circulation in response to a stimulus, and are nearly equallyrapidly dissipated when the release of adrenaline is slowed to baselevels in vivo. While these effects pass within seconds or at most a fewminutes, the compounds of the present invention typically persist intheir action for an interval of up to about two and often four hours.

As those of ordinary skill in the art will recognize, these features areconsistent, in part, with the high binding affinities of the presentcompounds.

As in the case of adrenaline and other compounds observed to activateβ₃-adrenoreceptors in vivo, the present compounds cause the breakdown ofadipose tissue at the cellular level, and increase release of glucoseinto the circulation and, separately, suppress the conversion ofcarbohydrates into glucose in the liver. Excess levels of glucose in theblood stream are excreted, primarily in the urine, either per se or as“ketone bodies” produced in the liver. These mechanisms are well studiedand characterized and do not form a part of the present invention. It isimportant in the case of diabetics to be aware of these effects and takethem into account in the management of diabetes to avoid the assumptionthat these conditions are an exacerbation of the diabetes or a failureof the diabetes therapies.

The trimethoxybenzyl portion of trimetoquinol was modified by replacingone or more of the methoxy groups with a variety of halogenatedsubstitutions. The effects of these modifications on the receptorbinding affinity of trimetoquinol analogs (Table 1) for human β₂adrenoreceptor, expressed in CHO cells and human TP receptors(platelets) were determined by radioligand competition binding assaysusing [¹²⁵I]-iodocynopindolol (ICYP) and [³H] SQ 29548 as radioligands,respectively.

Most of the modifications made on the trimethoxybenzyl portion oftrimetoquinol resulted in enhancement of β₂ Adrenoreceptor affinity.Previously, it was shown that replacement of the 3′ and 5′-methoxygroups of trimetoquinol with iodines [i.e., 1 (pKi=7.36) 2 (pKi=8.69)]resulted in a more than 20-fold increase in affinity, Fraundorfer, P.F.; Fertel, R. H.; Miller, D. D.; Feller, D. R. “Biochemical andpharmacological characterization of high-affinity trimetoquinol analogson guinea pig and human beta adrenergic receptor subtypes: evidence forpartial agonism” J Pharmacol Exp Ther 1994, 270, 665-74. In the presentstudy, complete replacement of the 3′-, 4′- and 5′-methoxy groups oftrimetoquinol (1) with iodine atoms to give the triiodo analog 21b(pKi=8.82) enhanced β₂-adrenoreceptor affinity 29-fold versustrimetoquinol (1) but with respect to 2, the additional iodinesubstituent at the 4′-position adds little to the binding affinity.

Studies on human β₂ Adrenoreceptor indicate that 4′-positionsubstituents of reflecting varying size and chemical properties are welltolerated. Replacement of the 4′-methoxy of 2 with an amino group [i.e.,2 ØØ21c (pKi=8.81)] did not significantly alter affinity, whilereplacement with a 4′-acetamido [i.e., 15 (pKi=8.06)] reduced affinityonly 4-fold. A similar replacement with a hydroxy (i.e., 18, pKi=7.93)reduced affinity about 5-fold as compared to 2. The receptor bindingpocket that interacts with substituents at the 4′-position seems to besufficiently large to accommodate the 4′-benzamido moiety of 26b(pKi=8.70). Interestingly, the diiodo analog 21a (pKi=9.52), which lacksa 4′-substituent, exhibits the most potent affinity with a Ki value inthe sub-nanomolar range.

It appears that one meta-iodo substituent is sufficient to retain highaffinity since removing one of the iodo groups of either 21c or 15[i.e., 21c ØØ24 (pKi=8.19) or 15 ØØ26a (pKi=8.11)] resulted in onlyminor shifts in affinity. To determine the nature (hydrophobic orelectronic) of the binding contributions of 3′ and 5′-substituents(methoxy and iodo), the bis-trifluoromethyl analog 27 was synthesized.While the hydrophobic property (π) of the trifluoromethyl group (π=0.88)is similar to iodine (π=1.12), this functional group exerts a muchstronger electron withdrawing effect. The binding affinity of thebis-trifluoromethyl analog 27 (pKi=5.36) was five orders of magnitudelower than the diiodo analog 21a. Thus, trifluoromethyl substituents atthe 3′- and 5′-positions abolish binding affinity. Since, atrifluoromethyl group is similar in size to an iodine atom, thesignificantly stronger electron withdrawing property of thetrifluoromethyl (σ_(p)=0.54 versus σ_(p)=0.18 for iodine) is likelyresponsible for the greatly reduced binding affinity of 27. The electronwithdrawing effect of the trifluoromethyl substituents on the π-electronsystem of the aromatic ring may interfere with its capability to formaromatic interactions with the receptor binding site. These aromaticinteractions may be more important for binding than hydrophobicinteractions.

Although replacement of the 3′ and 5′-methoxy groups of trimetoquinol 1,with iodine atoms (i.e., 2) resulted in a 21-fold increase in β₂adrenoreceptor affinity, a similar increase in binding affinity was notobserved at β₁ adrenoreceptor (Table 2). As a result, the diiodo analog2 exhibits moderate (ca. 40-fold) selectivity for β₂ adrenoreceptorversus β₁ adrenoreceptor. More importantly, the influence of a4′-substituent is markedly different for β₂ adrenoreceptor versus β₁adrenoreceptor. While the absence of a 4′-substituent (i.e., 21a) doesnot significantly alter β₁ Adrenoreceptor affinity (pKi=6.74), the samefeature increased β₂ Adrenoreceptor affinity. Consequently, analog 21adisplays more than 600-fold selectivity for β₂ Adrenoreceptor versus β₁Adrenoreceptor, and is the most selective trimetoquinol analog yetreported. These results indicate a remarkable difference in the receptorbinding site or pocket of β₂- and β₁ adrenoreceptor that interacts withsubstituents at the 4′-position of trimetoquinol analogs.

In general, replacement of the 3′ and 5′-methoxy groups of trimetoquinol(1, pKi=6.79) with iodine to give analog 2 (pKi=7.33) resulted in only aslight increase (3-fold) in affinity. However, replacement of all threemethoxy groups of trimetoquinol with iodines to give the triiodo analog21b (pKi=4.22) practically abolished binding to TP receptors. Inaddition, demethylation of the 4′-methoxy substituent of 2 to give 18(pKi=4.72) resulted in a similar 380-fold reduction in binding affinity.The very low binding affinity of 18 is in contrast to a recentobservation, Christoff, J. J. “Part 1: Synthesis of arylalkylguanidinesas dopamine agonists, Part 2, Section A: Modifications of trimetoquinoland the effects on beta-adrenergic and thromboxane A₂ receptor system,Section B: Approaches to the asymmetric synthesis of irreversiblybinding iodinated derivatives of trimetoquinol.” Ph. D. Thesis, The OhioState University, 1993, where6,7-dihydroxy-1-(4′-hydroxy-3′-nitrobenzyl)-1,2,3,4-tetrahydroisoquinolineexhibited good binding affinity. By contrast, substitution of the samemethoxy group with an amino moiety (i.e. 21c, pKi=6.73) resulted in onlya 3-fold decrease in affinity. Interestingly, removal of the4-′substituent of 2 or 21c to give 21a (pKi=6.75) did not affect bindingaffinity significantly. Acetylation of the 4′-amino group of 21c wasalso tolerated as 15 (pKi=6.45) displayed binding affinity similar to21c. Thus, while a primary amine, acetamide, or a methoxy group istolerated at the 4′-position, a free hydroxy group or an iodo group isdetrimental to binding affinity. Removal of one of the iodines of 21cand 15 to give 24 (pKi=6.00) and 26a (pKi=5.83), respectively, resultedin 5-fold decrease in binding affinity, suggesting that hydrophobicinteractions of 3′ or 5′-substituents contribute to binding. However,replacement of the 3′ and 5′-iodo groups of 21a with similarlyhydrophobic trifluoromethyl substituents resulted in drastic reductionin binding affinity. As with β₂ adrenoreceptor, in terms of contributionto overall binding affinity, hydrophobic interactions appear secondaryto aromatic interactions.

Synthesis of Thiazolopyridine Derivatives

The preparation of 2-amino-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridineshas been well documented in the literature (Thomae, K.4,5,6,7-Tetrahydrothiazolo[5,4-c]pyridines. Neth. Appl. 6 610 324, 1967;Chem. Abstr. 1968, 68, 49593p. Thomae, K. AnalgesicTetrahydrothiazolo[5,4-c]pyridines. Fr. Addn. 94 123, 1969; Chem. Abstr.1970, 72, 100685g. Hantzsch, A.; Traumann, V. Amidothiazole ausSulfoharnstoff und Halogenisirten Ketonen, resp. Aldehyden, Berichte1888, 21, 938-941). They are constructed by two approaches: a)Pictet-Spengler reaction—the condensation and subsequent cyclizationbetween an aldehyde and 2-(2′-amino-4′-thiazolyl)ethylamine derivatives;and b) Hantzsch thiazole synthesis—the condensation and subsequentcyclization between an α-bromopiperidone derivative and thiourea (FIG.3).

However, it was envisioned that both of these approaches would not meetour synthetic challenge. The Pictet-Spengler reaction would necessitatethe use of an inherently unstable substituted phenylacetaldehydewhereas, the required α-bromopiperidone for Hantzsch thiazole synthesisis not readily accessible synthetically. Alternatively, theBischler-Napieralski reaction (FIG. 3) is an attractive approach for thesynthesis of our designed TMQ analogs, because the required substitutedphenylacetic acids are stable, and readily accessible. TheBischler-Napieralski reaction is routinely used to preparedihydroquinolines (Whaley, W. M.; Govindachari, T. R. The Preparation of3,4-Dihydroisoquinolines and Related Compounds by theBischler-Napieralski Reaction, Org. React. 1951, VI, 74-150).

According to Timmerman's synthetic scheme (Eriks, J. C.; Van der Goot,H.; Sterk, G. J.; Timmerman, H. Histamine H₂-Receptor Agonists.Synthesis, in Vitro Pharmacology, and Qualitative Structure-ActivityRelationships of Substituted 4- and 5-(2-Aminoethyl)thiazoles, J. Med.Chem. 1992, 35, 3239-3246), compound 14, which is the starting amine forthe Bischler-Napieralski approach has been prepared (Scheme 1).

The transformation from 12 to 13 did not proceed in good yield asdescribed. Instead, the procedure described by Sprague et al (Sprague,J. M.; Land, A. H.; Ziegler, C. Derivatives of 2-Amino-4-methylthiazole,J. Am. Chem. Soc. 1946, 68, 2155-2159) converted 12 to 13 almostquantitatively.

Scheme 2 depicts the synthesis of analogs 7 and 9. Under theSchotten-Baumann condition, substituted phenylacetic acids 15 or 16(Harrold, M. W.; Gerhardt, M. A.; Romstedt, K.; Feller, D. R.; Miller,D. D. Synthesis and Platelet Antiaggregatory Activity of TrimetoquinolAnalogs as Endoperoxide/Thromboxane A₂ Antagonists, Drug Des. Deliv.1987, 1, 193-207) was allowed to react with compound 14. The amideprecursors 17 and 18 were obtained and each was treated with POCl₃ inrefluxing acetonitrile, and the putative dihydro intermediate wasreduced in situ with NaBH₄, giving final compounds 7 and 9 which werepurified by crystallization or column chromatography on silica gel.

The acetamido analog 10 was prepared according to Scheme 3. Acetylationof 18 with acetic anhydride gave precursor 19 that was then subjected toPOCl₃ and NaBH₄. Compound 10 was isolated as its maleic acid salt.

Analog 11 (Scheme 4) is a derivative of2-amino-4,5,6,7-tetrahydrothiazolo[4,5-c]pyridine that is an unknownheterocyclic system. Amide precursor 21 has been prepared from compound20 and 3,4,5-trimethoxyphenylacetic acid under Schotten-Baumanncondition.

Compound 20 was synthesized according to literature scheme (Scheme 5)(Eriks, J. C.; Van der Goot, H.; Sterk, G. J.; Timmerman, H. HistamineH₂-Receptor Agonists. Synthesis, in Vitro Pharmacology, and QualitativeSturcture-Activity Relationships of Substituted 4- and5-(2-Aminoethyl)thiazoles, J. Med. Chem. 1992, 35, 3239-3246).

However, the conversion from the α-bromoaldehyde 26 to 2-aminothiazole27 was again achieved effectively by using the procedure of Sprague etal (Sprague, J. M.; Land, A. H.; Ziegler, C. Derivatives of2-Amino-4-methylthiazole, J. Am. Chem. Soc. 1946, 68, 2155-2159). Usingvarious conditions (Whaley, W. M.; Govindachari, T. R. The Preparationof 3,4-Dihydroisoquinolines and Related Compounds by theBischler-Napieralski Reaction, Org. React. 1951, VI, 74-150; Kametani,T.; Fukumoto, K.; Fujihara, M. Studies on the Syntheses of HeterocyclicCompounds. Part CDLIV. Abnormal Dienone-Phenol Rearrangement ofProcularine, J. Chem. Soc. Perkin Trans. I 1972, 394-396; Rice, K. C.;Brossi, A. Expedient Synthesis of Racemic and Optically ActiveN-Norreticuline and N-Substituted and 6′-Bromo-N-norreticulines, J. Org.Chem. 1980, 45, 592-601) of Bischler-Napieralski reaction, attempts tocyclize the amide precursor 21 proved to be unsuccessful. However, ithas been reduced by BH₃ to give the open chain analog 24 that has alsobeen examined in all three human β-AR subtypes. Similarly, the acetamidoamide precursor 22 also failed to give the cyclized product under thereaction condition described.

Competitive Binding Studies

The competitive binding studies indicate that the compounds of thepresent invention are reversibly bound and confirms that they areequilibrium competitive binding species, No evidence of covalent bondingor other non-equilibrium binding mechanisms to the receptor sites isseen.

Binding to the β₁ adrenoreceptor, β₂ adrenoreceptor and the TP receptorsites is low, indicating that few side effects associated with thesereceptors is observed.

Binding to other types of receptors is unlikely.

Biochemical actions other than those associated with β₃-adrenoreceptorbinding and agonist activity are not observed. In particular, thecompounds of the present invention exhibit low acute toxicities, lowlong-term subacute toxicity, no evidence of receptor down regulation orother loss of effectiveness over time, and no indications to date ofadverse side reactions or side effects, short term or long term, whichwould represent contraindications for the indicated use.

The chemical properties and stability of the compounds permits theirformulation into substantially any suitable vehicle or carrierconsistent with the intended mode of administration. Those of ordinarylevels of skill in the pharmaceutical industry are fully capable ofdevising appropriate carriers for the administration of the compoundsconsistent with the intended mode of administration, and such carriersare employed in the present invention, but are not per se an inventivepart thereof.

The compounds of the present invention can be administered effectivelyby any route or modality consistent with the administration ofwater-soluble, polar pharmaceutical compounds. Administration may beoral, injectable (via im, iv, ip and subcutaneous, injections), or maybe implanted for sustained release by employment of known implantablesystems for the administration of bioactive agents. Absorption fromsuppositories is also effective, although generally limited by patientreluctance.

Topical administration is also effective, although provision must bemade for a suitable skin transport agent to be associated with thecompounds to assure that an effective level of the compounds areadministered to provide useful systemic levels.

Oral administration and, in suitable cases, implantable sustainedrelease systems are the preferred mode of administration. Implants areparticularly effective for those with acute obesity, for those who areinconsistent and/or non-compliant with scheduled oral dosages, andrelated circumstances. For general usage, oral administration willordinarily be preferred.

At the outset of administration, the compounds of the present inventionproduce marked weight loss in over-weight subjects, often at rates ofgreater than one pound per day and in acute subjects, at rates greaterthan two pounds per day. The rate is generally sustained until the levelof adipose tissue is markedly reduced, and the loss of weight and fattytissue slows until, at an equilibrium point which is directly related todosage levels, the body weight of the subject stabilizes. The dosagelevel may require adjustment from time to time to attain a suitableequilibrium level, which may be suitably defined by the percentage ofbody fat, the “body mass index” as that term is generally defined in themedical literature, or by other known factors.

If the compounds of the present invention are withdrawn, unless“semi-permanent” metabolic changes are induced as hypothesized below,the benefits of the present invention will be lost over time, and thebody weight and body fat will, unregulated, tend to return to its formerlevel.

Substantially all the adverse effects of over-weight and obesity will beeliminated, or at the least be materially reduced, as the levels offatty tissues and body mass are reduced.

The problems of glucose intolerance, insulin resistance and Type IIdiabetes (non-insulin dependent diabetes), in particular, will bereduced in magnitude or eliminated. In particular, the adverse andprogressive effects of such conditions will generally be arrested, therisks of non-compliance with specific treatments and dietary managementwill be reduced or eliminated, and the causes of such conditions may, insome cases, be moderated or even reversed.

As body fat is reduced, and body mass is reduced, the load on joint inthe body will be reduced, which may produce beneficial palliation of theeffects of osteo-arthritis, rheumatoid arthritis and other jointdisorders and sources of pain. Those having limited mobility associatedwith obesity will be better able to exercise and improved mobility canbe expected to result.

In most uses, the present invention will produce improved psychologicalprofiles in those concerned with body image and appearance. Such effectsare virtually always healthy and beneficial developments.

As the level of body fat declines, and so long as serum levels ofglucose are kept low, there will generally be an increase in themetabolism of dietary fat for the production of catabolic energyrequirements. A decline in serum cholesterol, low density lipids, totalserum lipids and related problems will occur. Theanti-hypercholersteremic effect is a highly desirable consequence of thepractice of the present invention. Such effects can be enhanced by adiet which limits carbohydrate intake. Over time, such effects may limitthe progress of or even reduce arterial occlusion and the incidence ofischemic and related consequences, including, among others, stroke andmyocardial infarction.

The increased reliance on dietary fats instead of carbohydrates, andparticularly serum glucose, may become so substantial, in fact, that insome cases intake of dietary fats will need to be increased to supportnormal catabolic energy requirements.

It is hypothesized that, over a long term, the effect of theadministration of the compounds of the present invention will so limitblood glucose and the conversion of blood glucose into fats that thebody will undergo a “semi-permanent” metabolic change, with increased(up-regulated) insulin receptors, decreased glucose intolerance(increased insulin responsiveness and efficiency generally), and reduced(down-regulated) mechanisms for the conversion of glucose and othercarbohydrates into adipose fat tissues. Increased reliance on dietaryfat as energy sources for catabolic processes would continue with thealteration of glucose responses and the hypocholesterolemic effectswould continue. These effects are not expected to occur until a suitableequilibrium state is attained, and will lag substantially behind bodymass and fatty tissue reduction, and will arise only as mitosis producesnew cells adapted to the equilibrium conditions, with environmentally“adjusted” receptor populations. These effects would be of particularbenefit in preventing or treating Type 11 diabetes and glucoseintolerance, in particular. These effects would alter the body massequilibrium point in a fundamental fashion, and would require reducingthe dosage of the compounds of the present invention and may, withsuitable dietary modifications and other behavioral modification, permitweaning the subject from reliance on the compounds altogether.

All indications to date suggest that the β₃-Adrenoreceptor agonists ofthe present invention are fully effective modulators of body weightwithout reliance on adjunctive or combination therapies. When suchadditional modalities, such as dietary restrictions and/or exercise, aredesirable for other reasons, or where the need for weight regulation andglucose modulation at the cellular level is needed in concert withtreatment of other disorders, such as diabetes and the like, there is noevidence that the present compounds and the utilization thereof conflictin any way with such additional or adjunctive treatments and therapies.

In particular, the present compounds do not interfere with theadministration of insulin or other agents to diabetic patients.

In addition, the present compounds are not inconsistent with specialdiets employed to regulate glucose intolerance, insulin intolerance andrelated disorders, including very low carbohydrate diets, very highprotein diets, and the like.

Where appetite and eating disorders are factors, the modalities of theaction of the present invention do not conflict with the usual andcommon treatments and therapies employed to control such conditions,including behavior modification, drug therapies and surgicalinterventions, although the present invention may in many caseseliminate the need to resort to such higher risk strategies and theproblems and consequences thereof may often be regulated by the presentinvention without resort to such additional strategies. The presentinvention results in an intrinsic suppression of appetite, tends totrigger satiety and tends to modulate the factors which promote appetiteand eating disorders, and is likely, over time, to result in substantialbehavior modification as the causes of such disorders are modulated. Theuse of appetite suppression is generally not indicated or required withthe present invention.

In general, when the compounds of the present invention areadministered, it is highly desirable to assure a balanced diet andadequate intake of vitamins and minerals. The nature of the action ofthe compounds of the present invention can accelerate the excretion ofboth oil soluble and water soluble vitamins and of minerals. Inaddition, it is advisable to maintain high fluid intake to aid in theexcretion of the high levels of glucose to be eliminated via thekidneys.

It is also appropriate in many cases to induce a suitable exerciseprogram to improve muscle tone, strength, mobility and agility inparallel with the practice of the present invention. While manyoverweight individuals exercise considerably, many more do not. Thecompounds of the present invention do not increase muscle strength orendurance, although the user will benefit from the reduced body mass andthe attendant load the muscles must carry, so that greater endurance and“perceived strength” or “relative strength” may increase and increasedactivity levels and exercise levels will often be a desirable sidebenefit of the practice of the invention.

Particularly those with limited joint functionality as an incident ofarthritic conditions and other like causes will find substantialpalliation and increased joint functionality as adipose tissue and bodymass are reduced and the load on the joints is reduced as a consequence.

The loss of body bulk may provide enhanced joint flexibility andincreased range of motion in some subjects who have been limited byobesity.

No absolute contraindications or adverse side effects of the compoundsof the present invention have been found to date.

Those with impaired liver or kidney function may face adverseconsequences from the increased levels of glucose in the circulation andthe increased load on the blood glucose processing and excretion. Suchindividuals may require reduced dosages (and more gradual effects) tolimit the loading on the liver and kidneys. The invention has not, todate, been tested with individuals with partially or totally incompetentkidneys, i.e. kidney deficient dialysis patients, but it appears thatthe present invention is not likely to exacerbate either the conditionswhich require reliance on dialysis or the risks of dialysis proceduresthemselves.

These compounds do not significantly bind or activate the β₁adrenoreceptor or the β₂ adrenoreceptor and thus do not produce theusual responses of agonists or blockers for these sites. There is noindication of significant or measurable binding to α-adrenoreceptors,and no indication of any activity consistent with such agonist orblocking activity. There is accordingly no hypertensive effect, novasodilator effect, and no bronchodilator effect observed in connectionwith the administration of the compounds of the present invention. Theseobservations are, of course, consistent with the high level ofselectivity of these compounds for the β₃-Adrenoreceptors.

EXAMPLES

The following specific examples demonstrate and illustrate the synthesisof the compounds of the present invention and intermediates prepared inthe course of the synthesis. The following apply to all the examplesrelated to the syntheses of compounds:

Melting points were determined on a Thomas-Hoover capillary meltingpoint apparatus and are uncorrected. Infrared spectra were recorded on aPerkin Elmer System 2000 FT-IR. Proton and carbon-13 magnetic resonancespectra were obtained on a Bruker AX 300 spectrometer (300 and 75 MHzfor ¹H and ¹³C, respectively). Chemical shift values are reported asparts per million (δ) relative to tetramethylsilane (TMS). Spectral dataare consistent with assigned structures. Elemental analyses wereperformed by Atlantic Microlab Inc., Norcross, Ga., and found values arewithin 0.4% of the theoretical values. Routine thin-layer chromatography(TLC) was performed on silica gel GHIF plates (250 m, 2.5×10 cm;Analtech Inc., Newark, Del.). Flash chromatography was performed onsilica gel (Merck, grade 60, 230-400 mesh, 60 Å). Tetrahydrofuran (THF)was dried by distillation from sodium metal, and acetonitrile (MeCN),CHCl₃ and methylene chloride (CH₂Cl₂) were dried by distillation fromβ₂O₅. All anhydrous solvents (except anhydrous Et₂O and THF) were storedover 3- or 4-Å molecular sieves.

TMQ Derivatives Example 1

N-(3,4-dimethoxyphenethyl)-4-nitrophenylacetamide

A solution of 3,4-dimethoxyphenethylamine (5.0 g, 27.6 mmol) and4-nitrophenylacetic acid (7.5 g, 41.4 mmol) in toluene (150 mL) washeated at reflux for 72 h in a flask equipped with a Dean-Stark trapunder an argon atmosphere. The solvent was evaporated in vacuo and theresidue was taken up in CH₂Cl₂ (200 mL). The solution was washedconsecutively with H₂O (100 mL), 10% HCl (2×100 mL), H₂O (2×100 mL), 10%NaHCO₃ (2×200 mL), H₂O (2×100 mL) and dried over MgSO₄. The solvent wasevaporated and the crude solid was recrystallized from EtOAc to give5.49 g (58%) of the product as ivory colored needles: mp 119-121° C.(lit.²² 130-132° C., ethanol-isopropanol); ¹H NMR (CDCl₃) δ8.16 (d,J=8.8 Hz, 2H, ArH), 7.37 (d, J=8.8 Hz, 2H, ArH), 6.73 (d, J=8.1 Hz, 1H,ArH), 6.65 (d, J=1.9 Hz, 1H, ArH), 6.60 (dd, J=8.1 & 1.9 Hz, 1H, ArH),5.40 (m, 1H, NH), 3.86 (s, 3H, OMe), 3.84 (s, 3H, OMe), 3.59 (s, 2H,CH₂), 3.51 (q, J=6.9 Hz, 2H, CH₂), 2.73 (t, J=6.9 Hz, CH₂); IR (KBr)3320 (NH), 1650 (C═O) cm⁻¹; Anal. (C₁₈H₂₀N₂O₅) C, H, N.

Example 2

N-(3,4-dim thoxyphenethyl)-3,5-bis-trifluoromethylphenylacetamide

A solution of 3,4-dimethoxyphenethylamine (2.72 g, 15 mmol) and3,5-bis-trifluoromethylphenylacetic acid (2.72 g, 10 mmol) in toluene(50 mL) was heated at reflux for 80 h in a flask equipped with aDean-Stark trap. The solvent was evaporated in vacuo and the residue wastaken up in CH₂Cl₂. The solution was washed consecutively with 0.1 N HCl(30 mL), H₂O (50 mL), 0.1 N NaOH (30 mL), H₂O (50 mL) and dried overMgSO₄. The solvent was evaporated and the crude solid was recrystallizedfrom toluene to give 3.44 g (79%) of the product as white needles: mp127-128° C.; ¹H NMR (CDCl₃) δ7.79 (s, 1H, ArH), 7.72 (s, 2H, ArH), 6.75(d, J=8.1 Hz, 1H, ArH), 6.67 (d, J=1.9 Hz, 1H, ArH), 6.61 (dd, J=8.1 &1.9 Hz, 1H, ArH), 5.55 (m, 1H, NH), 3.85 (s, 3H, OMe), 3.84 (s, 3H,OMe), 3.58 (s, 2H, CH₂), 3.52 (q, J=6.9 Hz, 2H, CH₂N), 2.75 (t, J=6.9Hz, CH₂); ¹³C NMR (CDCl₃) δ168.72, 149.20, 147.87, 137.28, 131.90,130.79, 129.47, 123.16, 121.20, 120.56, 111.72, 111.27, 55.83, 42.85,40.90, 34.97; IR (KBr) 3323 (NH), 1651 (C═O) cm⁻¹; Anal. (C₂₀H₁₃F₆NO₃)C, H, N.

Example 3

6,7-Dimethoxy-1-(4-nitrobenzyl)-1,2,3,4-tetrahydroisoquinoline

A mixture of 5a (8.0 g, 23.2 mmol) and POCl₃ (15.6 mL, 167.4 mmol) indry MeCN (160 mL) was heated at reflux for 4 hours. The solvent wasevaporated in vacuo to give a glassy residue which was taken up inmethanol (250 mL) and evaporated to dryness three times until theresidue was a solid. The solid residue was dissolved in MeOH (250 mL)then cooled in an ice bath. Excess NaBH₄ (17.56 g, 167.4 mmol) wascarefully added in portions. The mixture was stirred at room temperatureovernight. The solvent was removed in vacuo and the solid residue waspartitioned in CH₂Cl₂ (250 mL) and H₂O (150 mL). The layers wereseparated and the H₂O layer was extracted with CH₂Cl₂ (100 mL). Thecombined organic fraction was washed successively with H₂O (2×50 mL), 2NNaOH (2×50 mL), H₂O (50 mL), and dried with Na₂SO₄. The solvent wasevaporated to give a reddish oil. The oil was taken up in a minimumamount of methanol. The product crystallized upon standing and wascollected by filtration (3.02 g, 40%): mp 134-36° C.; ¹H NMR (CDCl₃)δ8.18 (d, J=8.7 Hz, 2H, ArH), 7.43 (d, J=8.7 Hz, 2H, ArH), 6.62 (s, 1H,ArH), 6.61 (s, 1H, ArH), 4.44 (dd, J=9.5, 4.1 Hz, ArCH—N), 3.87 (s, 3H,OMe), 3.84 (s, 3H, OMe), 3.28 (dd, J=13.7, 4.1 Hz, 1H, ArCH₂), 3.23-3.15(m, 1H, NCH), 3.04 (dd, J=13.7, 9.5 Hz, 1H, ArCH), 3.00-2.91 (m, 1H,NCH), 2.71 (m, 2H, ArCH₂); Anal. (C₁₈H₂₀N₂O₄) C, H, N.

Example 4

6,7-Dimethoxy-1-(3,5-bis-trifluoromethybenzyl)-1,2,3,4-tetrahydroisoquinolinehydrochloride

The amide 5c (1.31 g, 3 mmol) was cyclized in the same manner as 6a (7mL of 1M HCl in ether was added to the methanolic solution of a crudeproduct) to give 6c (0.84 g, 60%) as a hydrochloride salt: mp 104-115°C. (MeOH-ether); ¹H NMR (CDCl₃) δ10.34 (bs, 2H, NH), 7.82 (s, 1H, ArH),7.75 (s, 2H, ArH), 6.61 (s, 1H, ArH), 5.87 (s, 1H, ArH), 4.77 (m, 1H,CH), 3.91 (m, 1H, CH), 3.84 (s, 3H, OMe), 3.47 (s, 3H, OMe), 3.44 (m,2H, CH), 3.28 (m, 2H, CH), 3.02 (m, 1H, CH); ¹³C NMR (CDCl₃) δ149.29,147.74, 138.74, 132.08, 130.39, 123.33, 123.07, 121.40, 111.71, 109.43,55.92, 55.38, 54.94, 40.46, 38.30, 24.80; IR (KBr) 3436 (NH), 1281, 1379(C—O) cm⁻¹. Anal. (C₂₀H₁₉F₆NO₂.HCl.0.5 H₂O) C, H, N.

Example 5

6,7-Dimethoxy-1-(4-nitrobenzyl)-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

A solution of6,7-dimethoxy-1-(4-nitrobenzyl)-1,2,3,4-tetrahydrisoquinoline (6a) (3.0g, 9.14 mmol) in dry THF (150 mL) was added to trifluoroacetic anhydride(20 mL) with stirring at 0° C. The mixture was stirred at roomtemperature overnight with the flask equipped with a CaCl₂ drying tube.The reaction mixture was poured onto ice (200 g) and the mixture stirredfor 30 minutes. CH₂Cl₂ (200 mL) was added and stirring was continued for10 minutes. The layers were separated and the organic layer was washedconsecutively with H₂O (50 mL), 0.2N NaOH (100 mL), H₂O, (100 mL), andthen dried with Na₂SO₄. The solvent was evaporated in vacuo to give ayellow solid. Recrystallization from EtOAc-MeOH gave 1.94 g (50%) ofyellow crystals: mp 162-64° C.; ¹H NMR (CDCl₃) δ8.14 (m, 2H, ArH), 7.28(m, 2H, ArH), 6.62 (s, 1H, ArH), 6.34 (s, 1H, ArH), 5.64 (t, J=6.7 Hz,ArCH—N), 3.87 (s, 3H, OMe), 3.72 (s, 3H, OMe), 3.3-3.6 (m, 2H, N-CH₂),3.25 (d, 2H, ArCH₂), 2.98-2.6 (m, 2H, ArCH₂); IR (KBr) 1686 (C═O), 1519,1340 (NO₂) cm⁻¹; MS m/e (m⁺): 423 (M+H, FAB). Anal. (C₂₀H₁₉F₃N₂O₅) C, H,N.

Example 6

6,7-Dibenzyloxy-2-tert-butoxycarbonyl-1-(4-nitrobenzyl)-1,2,3,4-tetrahydroisoquinoline

A solution of (Boc)₂O (2.84 g, 13 mmol) in THF (10 mL) was added to acold mixture (ice bath) of isoquinoline 6b (6.20 g, 12 mmol) in THF (100mL) and 1N NaOH solution (30 mL). The ice bath was removed and stirringwas continued at room temperature overnight. THF was evaporated underreduced pressure, water was added and the product was extracted withCH₂Cl₂, dried over MgSO₄, filtered and evaporated again. The oilyresidue was dissolved in ether and put in a refrigerator. Pink crystalswere filtered and washed with ether to give 6.00 g (86%) of the titlecompound: mp 150-152° C.; ¹H NMR (CDCl₃) δ(the spectrum consists of tworotamers of 5:4 ratio) 8.11 and 8.06 (d, J=8.2 Hz, 2H, ArH), 7.47-7.27and 7.21-7.11 (m, 12H, ArH), 6.70 and 6.67 (s, 1H, H-5), 6.56 and 6.44(s, 1H, ArH), 5.27-4.96 (m, 5H, CH₂O+CH), 4.12 and 3.74 (m, 1H, CH),3.25-3.00 (m, 3H, CH, CH₂Ar), 2.87-2-60 (m, 1H, CH), 2.57-2.37 (m, 1H,CH), 1.38 and 1.25 (s, 9 H, t-Bu); IR (KBr) 1688 (C═O), 1518, 1345 (NO₂)cm⁻¹. Anal. (C₃₅H₃₆N₂O₆) C, H, N.

Example 71-(4-Aminobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

A solution of 7a (5.20 g, 12.24 mmol) in ethyl acetate (200 mL) washydrogenated (60 psi) over 5% Pd/C (1 g) for 2 hours. The catalyst wasremoved by filtration and the filtrate was evaporated to dryness to givea beige solid. Recrystallization from ethyl acetate and hexane gave 4.20(87%) of the product as light pink to white crystals: mp 157-160° C.; ¹HNMR (CDCl₃) δ6.88 (d, 2H, ArH), 6.59(d, 3H, ArH), 6.32 (s, 1H, ArH),5.53 (t, 1H, ArCH—N), 3.99 (m, 1H, CH), 3.86 (s, 3H, OMe), 3.71 (s, 3H,OMe), 3.60 (bs, 2H, NH₂), 3.42-3.56 (m, 2H, CH), 2.85-3.20 (m, 3H, CH),2.59-2.73 (m, 1H, CH); IR (KBr) 3370 (m, NH₂), 1689 (C═O) cm⁻¹; MS m/e(m+): 395 (M+H, FAB). Anal. (C₂₀H₂₁F₃N₂O₃)C, H, N.

Example 8

1-(4-Aminobenzyl)-6,7-dibenzyloxy-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline

The nitro compound 7b (6.00 g, 10.3 mmol) was dissolved in EtOAc (230mL) in a Parr bottle. The solution was charged with a slurry of Raney-Ni(4 mL) and hydrogenated at 50 psi for 3 h. The solution was filteredthrough celite and evaporated to give 5.10 g (90%) of the crudecompound. The product was purified by flash chromatography (silica gel,hexane-EtOAc 2:1) to give a foamy glassy solid (4.51 g, 71%); ¹H NMR(CDCl₁₃) δ(the spectrum consists of 2 rotamers of 5:2 ratio) 7.48-7.24(m, 10H, 2×Ph), 6.82 (m, J=8.2 Hz, ArH, 6.68 and 6.64 (s, 1H, ArH), 6.58(m, J=8.2 Hz, 2H, ArH), 6.49 and 6.32 (s, 1H, ArH), 5.12-4.81 (m, 5H,2×CH₂O+CH), 4.18-4.08 and 3.81-3.71 (m, 1H, CH), 3.27-3.09 (m, 1H, CH),3.00-2.60 (m, 3H, CH₂Ar, CH), 2.59-2.40 (m, 1H, CH), 1.43 and 1.32 (s,9H, t-Bu); IR (KBr) 3451 and 3365 (NH₂), 1684 (C═O), 1624 (NH bend),1517 (C═C Ar) cm⁻¹. Anal. (C₃₅H₃₈N₂O₄) C, H, N.

Example 9

1-(4-Amino-3-iodobenzyl)-6,7-dibenzyloxy-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline

A mixture of isoquinoline 8b (1.11 g, 3.2 mmol), BTMACl₂I (1.1 g, 3.2mmol), CaCO₃ (0.44 g, 4.4 mmol) in CH₂Cl₂ (50 mL) and MeOH (20 mL) wasstirred overnight at room temperature. CaCO₃ was filtered and washedwith CH₂Cl₂. The filtrate was washed with solution of Na₂S₂O₃ (×2), H₂O(×2), dissolved in CHCl₃ and EtOH and concentrated till the beginning ofcrystallization to give 1.59 g (81%) of title compound as pink crystals:mp 169-171° C.; ¹H NMR (CDCl₃) δ(the spectrum consists of 2 rotamers of2:1 ratio) 7.47-7.25 (m, 11H, ArH), 6.81 (dd, J=8.1, J=1.6 Hz, 1H, ArH),6.70-6.59 (m, 2H, ArH), 6.49 and 6.30 (s, 1H, ArH), 5.20-5.85 (m, 5H,CH₂O+CH), 4.13 and 3.74 (m, 1H, CH), 4.01 (s, NH₂), 3.30-3.10 (m, 1H,CH), 2.96-2.59 (m, 3H, CH₂Ar+CH), 2.59-2.43 (m, 1H, CH), 1.44 and 1.32(s, 9H, t-Bu); IR (KBr) 3453 and 3334 (NH₂), 1667 (C═O), 1627 (NH bend),1520 and 1498 (C═C Ar) cm⁻¹. Anal. (C₃₅H₃₇IN₂O₄) C, H, N.

Example 10

1-(4-Amino-3,5-diiodobenzyl)-2-trifluoroacetyl-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

To a solution of 8a (0.1 g, 2.54 mmoL) in CH₂Cl₂ (50 mL) and methanol(20 mL)was added BTMACl₂I (2.0 g, 5.77 mmoL) and CaCO₃ (2.0 g). Themixture was stirred overnight at room temperature. A second portion ofBTMACl₂I (0.97 g, 2.8 mmol) was added and stirring was continuedovernight. Analysis of the reaction indicated a mixture of mono- anddiiodinated products. The reaction mixture was filtered. The filtratewas washed consecutively with aqueous 5% Na₂S₂O₃ (40 mL) and water (50mL), then dried with Na₂SO₄. Evaporation of the solvent gave a reddishglassy solid. The desired diiodinated product was purified from thecrude mixture by flash chromatography (CH₂Cl₂:EtOAc, 9:1). Theappropriate fractions were combined and evaporated in vacuo to give 0.72(44%) of the product as a white solid: mp 183-184.5° C.; 1H NMR (CDCl₃)δ7.37 (s, 2H, ArH), 6.61 (s, 1H, ArH), 6.29 (s, 1H, ArH), 5.43 (m, 1H,ArH), 4.56 (bs, 2H, NH₂), 3.87 (s, 3H, OMe), 3.73 (s, 3H, OMe), 3.60 (m,1H, CH), 2.91 (m, 4H, CH), 2.70 (m, 1H, CH); IR (KBr) 3429, 3348 (NH),1685 (C═O) cm⁻¹; Anal. (C₂₀H₁₉F₃I₂N₂O₃) C, H, N.

Example 11

4′,4″-Azobis[1-(4-Amino-3,5-diiodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline]

Was isolated from the above mixture as a bottom spot, deep-purple solid:mp 229-232° C.; 1H NMR (CDCl₃) δ7.78 (s, 2H, ArH), 6.65 (s, 1H, ArH),6.18 (s, 1H, ArH), 5.53 (dd, J=7.9, 5.6 Hz, 1H, ArH), 3.99 (m, 1H, CH),3.88 (s, 3H, OMe), 3.74 (m, 1H, CH), 3.72 (s, 3H, OMe), 3.16 (dd,J=13.0, 5.3 Hz, 1H, CH), 2.96 (m, 2H, CH), 2.80 (dt, J=16.2, 4.5 Hz, 1H,CH); ¹³C NMR (CDCl₃) δ156.14, (q) 148.89, 148.54, 147.59, 142.27,141.53, 125.60, 125.05, 116.47 (q), 111.28, 110.42, 89.83, 56.15, 56.01,55.54, 40.88 (q), 40.60, 28.45; IR (KBr) 1688 (C═O), 1520 (C═C Ar) cm⁻¹;Anal. (C₄₀H₃₄F₆I₄N₄O₆) C, H, N.

The same product was obtained via diazotization of 10a (0.32 g, 0.5mmol, see below) and stirring overnight with 20 mL of 6% H₂SO₃ at roomtemperature, yield 0.03 g (10%) after flash column chromatography.

Example 12

4′,4″-Azobis[1-(4-Amino-3,5-diiodobenzyl)-6,7-dimethoxy-1,2,3,4-ttrahydroisoquinoline]

A solution of azo-compound 11 (0.26 g, 0.2 mmol) in 35 mL of MeOH and0.85 g of K₂CO₃ in 11 mL was refluxed for 4 h and evaporated. Flashchromatography on silica gel (CH₂Cl₂, CH₂Cl₂-MeOH 50:1, 30:1) gave 0.15g (70%) of the product, mp 176-177° C. (dec.); 1H NMR (300 MHz, CDCl₃)δ7.96 (s, 2H, ArH), 6.62 (s, 1H, ArH), 6.61 (s, 1H, ArH), 4.20 (dd,J=9.6, 4.0 Hz, 1H, ArH), 3.87 (s, 3H, OMe), 3.86 (s, 3H, OMe), 3.10-3.30(m, 2H, CH), 3.00 (m, 1H, CH), 2.68-2.90 (m, 2H, CH); ¹³C NMR (CDCl₃)δ148.43, 147.75, 147.21, 144.05, 141.87, 129.76, 127.43, 112.03, 109.34,90.43, 56.61, 56.16, 55.88, 41.65, 40.51, 29.36; IR (KBr) 1515 (C═C, Ar)cm⁻¹; Anal. (C₃₆H₃₆I₄N₄O₄) C, H, N.

Example 13

1-(4-Acetamido-3,5-diiodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

A solution of acetyl chloride (0.80 g, 7.8 mmol) in dry THF (2 mL) wasadded dropwise to a stirred solution of 10a (1.0 g, 1.56 mmol), Et₃N(0.40 g, 7.8 mmol), and N,N-dimethylaminopyridine (DMAP, @10 mg) in dryTHF (20 mL) at 0° C. under an argon atmosphere. After the addition thereaction mixture was allowed to warm to room temperature and stirringwas continued overnight (14 h). The reaction was quenched with H₂O (20mL) and stirred for 30 min. The solution was extracted with Et₂OAc (3×75mL). The organic extract was washed with H₂O (20 mL), dried (Na₂SO₄) andevaporated in vacuo to give a tan solid. Recrystallization of the crudeproduct from EtOH and H₂O gave 0.93 g (87%) of the title compound aslight beige needles: mp 218-219° C.; ¹H NMR (CDCl₃) δ7.5-7.75 (bm, 2H,ArH), 6.96 (s, 1H, CONH), 6.62 (s, 1H, ArH), 6.24 (s, 1H, ArH), 5.47 (t,J=6.7 Hz, 1H, CH)3.98 (m, 1H, CH), 3.87 (s, 3H, OMe), 3.73 (s, 3H, OMe),2.83-3.18 (m, 4H, CH), 2.74, (m, 1H, CH), 2.22 (s, 3H, Ac); ¹³C NMR(CDCl₃) δ168.14, 156.02, (q), 148.39, 147.68, 140.58, 140.31, 139.35,125.71, 124.85, 116.4 (q), 98.73, 56.09, 55.93, 55.44, 40.63 (q), 40.48,28.43, 23.62 IR (KBr) 3387 (NH), 1683 (CO). Anal. (C₂₂H₂₁F₃I₂N₂O₄) C, H,N.

Example 14

1-(4-Acetamido-3,5-diiodobenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolineHydrochloride

A solution of 13 (1.22 g, 1.78 mmol) in methanol (60 mL) was added to asolution of K₂CO₃ (5.6 g) in 80 mL of 1:1 methanol and water. Themixture was stirred at room temperature for 3 hours. The resultingsolution was concentrated then extracted with ethyl acetate (3×80 mL).The organic solution was dried (Na₂SO₄) and evaporated in vacuo to givethe 0.79 g (75%) of the product as the free base. The free baseconverted to the hydrochloride salt and recrystallized from anhydrousethanol and ethyl ether: mp 196-200° C. (dec); ¹H NMR (DMSO-D₆) δ9.85(s, 1H, CONH), 9.35 (bm, 2H, NH⁺), 7.98 (s, 1H, ArH), 7.96 (s, 1H, ArH),6.78 (s, 1H, ArH), 6.65 (s, 1H, ArH), 4.65 (bm, 1H, CH), 3.83 (s, 3H,OMe), 3.73 (s, 3H, OMe) 3.35-3.43 (m, 1H, CH), 2.8-3.2 (m, 5H, CH), 2.01(s, 3H, Me); IR (KBr) 1677 (C═O), 1514 (C═C Ar) cm⁻¹; MS m/e (m+): 592(M—HCl, El). Anal. (C₂₀H₂₂I₂N₂O₃.HCl.0.5Et₂O) C, H, N.

Example 15

1-(4-Acetamido-3,5-diiodobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineHydrobromide

To a solution of 14 (0.50 g, 0.88 mmol) in dry CH₂Cl₂ (50 mL) at 0° C.(ice bath) was added dropwise 1M BBr₃ (4 mL, 4 mmol) in CH₂Cl₂ under anargon atmosphere. The mixture was then allowed to reach room temperatureand stirring was continued overnight. The reaction mixture was cooledwith an ice bath and methanol (20 mL) was added carefully. The solutionwas stirred for 10 minutes then evaporated in vacuo. This was repeatedfour times to give a solid which was stirred with ether overnight. Thecrude product was collected by filtration and recrystallized frommethanol and ethyl ether to give 0.51 g (90%) of the desired product asan off-white solid: mp 202-206 (dec) ° C.; ¹H NMR (DMSO-D₆) δ9.82 (s,1H, CONH), 9.15 (bm, 1H, OH), 8.91 (bm, 2H, NH⁺), 8.55 (bm, 1H, OH),7.97 (s, 1H, ArH), 7.94 (s, 1H, ArH), 6.71 (s, 1H, ArH), 6.56 (s, 1H,ArH), 4.66 (bm, 1H, CH), 3.27-3.35 (m, 2H, CH), 3.10-3.16 (m, 2H, CH),2.70-2.93 (m, 4H, CH), 2.02 (s, 3H, Me); ¹³C NMR (CD₃OD) δ172.51(C═O),147.04 and 145.89 (C-6 and C-7), 142.34 (C₄′), 141.90 and 141.73 (C-2′and C-6′), 140.18 (C-1′), 123.67 and 123.09 (C-4a and C-8a), 116.32(C-5), 114.11 (C-8), 100.61 and 100.46 (C-3′ and C-5′), 57.51 (C-1),41.10 (C-3), 39.31 (CH₂Ar), 25.70 (C-4) 23.09 (COCH₃); IR (KBr) 1652(CO), 1524 (C—N) cm⁻¹; MS m/e (m+): 565 (M+H, FAB). Anal.(C₁₈H₁₈N₂O₃I₂.HBr.0.25 Et₂O) C, H, N.

Example 16

1-(4-Diacetamido-3,5-diiodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

A solution of 10a (0.70 g, 1.08 mmol) in acetic anhydride (10 mL) washeated at reflux for 2 h. The solvent was evaporated in vacuo to give anoily residue. The residue was taken up in hot ethanol. The productcrystallized upon cooling to give 0.78 g (99%) of the product as whitecrystals: mp 190-192° C.; ¹H NMR (CDCl₃) 7.70 (s, 2H, ArH), 6.64 (s, 1H,ArH), 6.39(s, 1H, ArH), 5.53 (t, J=6.7 Hz, 1H, CH), 3.96 (m, 1H, CH),3.87 (s, 3H, OMe), 3.79 (s, 3H, OMe), 2.68 (m, 1H, CH), 2.94-3.07 (m,3H, CH), 2.77 (m, 1H, CH), 2.28 (s, 6H, Ac); ¹³C NMR (CDCl₃) δ71.23,155.93 (q), 148.48, 147.86, 142.66, 141.36, 141.12, 125.65, 124.83,116.31 (q), 111.14 109.88, 99.21, 56.08, 55.93, 55.31, 40.58, 40.44 (q),28.43, 26.60; IR (KBr) 1719, 1683 (C═O), 1235, 1207 (C—O) cm⁻¹. Anal.(C₂₄H₂₃F₃I₂N₂O₅) C, H, N.

Example 17

6,7-Dihydroxy-1-(4-hydroxy-3,5-diiodobenzyl)-1,2,3,4-tetrahydroisoquinolineHydrobromide

Hydrochloride 17¹⁰ (0.21 g, 0.28 mmol) was dissolved in CHCl₃ and washedwith 1N NaOH, organic layer was separated, washed with water and driedover MgSO₄. The solution was filtered, evaporated and dried undervacuum. The residue was dissolved in CH₂Cl₂ (4 mL) and 1M BBr₃ in CH₂Cl₂(1.39 mL, 1.39 mmol) was added at −78° C. under argon atmosphere. Themixture was stirred overnight at room temperature followed by MeOH (1mL) was added and stirred for 5 h. The resulting solution was evaporatedwith MeOH 5 times and the residue was recrystallized from MeOH-ether togive 0.078 g (45%) of white crystals: mp 235-237° C. (dec.); ¹H NMR(DMSO-D₆) δ9.50 (s, 1H, OH), 9.14 (s, 1H, OH), 8.89 (s, 1H, OH), 8.78(br. s, 1H, NH⁺), 8.43 (br. s, 1H, NH⁺), 7.76 (s, 2H, ArH, 6.64 (s, 1H,ArH), 6.55 (s, 1H, ArH), 4.55 (m, 1H, CH), 3.40-3.05 (m, 3H, CH),2.92-2.68 (m, 3H, CH); ¹³C NMR (CD₃OD) δ156.59 (C-4′), 146.96 and 145.85(C-6 and C-7), 141.69 (C-2′ and C-6′), 132.30 (C-1′), 123.71 and 123.24(C-4a and C-8a), 116.25 (C-5), 114.14 (C-8), 85.85 (C-3′ and C-5′),57.55 (C-1), 41.08 (C-3), 39.12 (CH₂Ar), 25.68 (C4); IR (KBr) 3600-2600(OH, NH), 1527 (C═C, Ar) cm⁻¹. Anal. (C₁₆H₁₅I₂NO₃.HBr.0.1Et₂O) C, H, N.

Example 18

1-(3,5-Diiodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

A solution of isoquinoline 10a (1.29 g, 2 mmol) in glacial acetic acid(30 mL) was added to a cold solution of NaNO₂ (0.19 g, 2.8 mmol) inconcentrated (d 1.84) H₂SO₄ (3.4 mL), the temperature was kept within0-5° C. The solution was poured into ice-water (60 g) and H₃PO₂ (12 ml)was added in 30 min. The cooling bath was removed and the solution wasallowed to stand at room temperature for 2 days. The precipitate wasfiltered, dried and chromatographed on silica gel (hexane-AcOEt 8:1).Recrystallization from AcOEt-hexane gave 0.50 g (40%) of whitecrystals.: mp 162-163° C.; 1H NMR (CDCl₃) δ7.93 (t, J=1.5 Hz, 1H, ArH),7.43 (d, J=1.5 Hz, 2H, ArH), 6.62 (s, 1H, ArH), 6.24 (s, 1H, ArH), 5.48(t, J=6.7 Hz, 1H, CH), 3.95 (m, 1H, CH), 3.87 (s, 3H, OMe), 3.72 (s, 3H,OMe), 3.61 (m, 1H, CH), 3.06-2.86 (m, 3H, CH), 2.70 (m, 1H, CH); ¹³C NMR(CDCl₃) δ155.98 (q) 148.46, 147.67 143.60, 141.25, 137.98, 125.86,125.00, 116.41 (q), 111.20, 110.19, 94.58, 55.96, 55.93, 55.37, 41.1340.61 (q), 28.44; IR (KBr) 1686 (C═O), 1541, 1520 (C═C Ar) cm−1. Anal.(C₁₈H₁₉I₂NO₂) C, H, N.

Example 19

1-(3,4,5-Triiodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

Compound 10a (1.29 g, 2 mmol) was diazotized in the usual manner. Theresulting solution was poured in ice-water (60 g) followed by KI (0.47g, 2.8 mmol) in water (10 mL) was added. The mixture was heated to 80°C. and allowed to cool. The precipitate was filtered, dried and purifiedby column chromatography (silica gel, hexane-AcOEt 3:1). Yield 0.51 g(34%): mp 215-216° C.; ¹H NMR (CDCl₃) δ7.59 (s, 2H, ArH, 6.63 (s, 1H,ArH), 6.31 (s, 1H, ArH), 5.46 (t, J=6.7 Hz, 1H, ArH), 3.93 (m, 1H, CH),3.88 (s, 3H, OMe), 3.75 (s, 3H, OMe), 3.61 (ddd, J=13.8, J=9.9, J=4.1Hz, 1H, CH), 3.02-2.85 (m, 3H, CH₂Ar+CH), 2.70 (dt, J=16.2, J=4.3 Hz,1H, CH); ¹³C NMR (CDCl₃) δ156.07 (q), 148.48, 147.71, 140.45, 139.90,125.67, 125.08, 118.91, 116.39 (q), 111.16, 110.08, 106.78, 55.97,55.10, 40.68 (q), 40.32 28.43; IR (KBr) 1685 (C═O), 1519 (C═C Ar) cm⁻¹.Anal. (C₂₀H₁₇F₃I₃NO₃) C, H, N.

Example 20

1-(3,5-Diiod benzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

A mixture of isoquinoline 19a (0.38 g, 0.6 mmol) in MeOH (35 mL) andK₂CO₃ (0.85 g) in water (11 mL) were refluxed for 1.5 h. MeOH wasevaporated and a white precipitate was filtered and dried. The crudeproduct was purified by flash chromatography (silica gel) using agradient (EtOAc-hexanes 1:2, EtOAc, EtOAc-MeOH 30:1) and recrystallizedfrom EtOAc-hexanes to give 0.25 g (76%) of white crystals: mp 122-124°C.; ¹H NMR (CDCl₃) δ7.94 (t, J=1.4 Hz, 1H, ArH), 7.60 (d, J=1.4 Hz, 2H,ArH), 6.60 (s, 1H, ArH), 6.57 (s, 1H, ArH), 4.10 (m, 1H, CH), 3.86 (s,3H, OMe), 3.84 (s, 3H, OMe), 3.18 (m, 1H, CH), 3.08 (dd, J=4.1 and 13.7Hz, 1H, CH), 2.95 (m, 1H, CH), 2.82-2.61 (m, 3H, CH); ¹³C NMR (CDCl₃)δ147.68, 147.17, 143.78, 143.15, 137.64, 129.86, 127.42, 111.98, 109.32,94.99, 56.57, 56.06, 55.87, 42.20, 40.55, 29.39; IR (KBr) 3325 (NH),1516 (C═C Ar) cm⁻¹ Anal. (C₁₈H₁₉I₂NO₂) C, H, N.

Example 21

6,7-Dimethoxy-1-(3,4,5-triiodobenzyl)-1,2,3,4-tetrahydroisoquinoline

A mixture of isoquinoline 19b (0.454 g, 0.6 mmol) in MeOH (35 mL) andK₂CO₃ in water (11 mL) were refluxed for 1.5 h. MeOH was evaporated anda white precipitate was filtered and dried. Recrystallization fromCHCl₃-hexane gave 0.300 g (76%) of white crystals: mp 168-170° C.(dec.); ¹H NMR (CDCl₃) δ7.79 (s, 2H, ArH), 6.60 (s, 1H, ArH), 6.58 (s,1H, ArH), 4.09 (dd, J=9.8, 3.8 Hz, 1H, CH), 3.86 (s, 3H, OMe), 3.85 (s,3H, OMe), 3.17 (m, 1H, CH), 3.04-2.88 (m, 2H, CH), 2.82-2.60 (m, 3H,CH); ¹³C NMR (CDCl₃) δ147.66, 147.15, 143.00, 139.68, 129.67, 127.42,118.18, 111.92, 109.14, 107.09, 56.35, 56.06, 55.85, 41.38, 40.56,29.35; IR (KBr) 3312 (NH), 1516 (C═C Ar) cm⁻¹. Anal. (C₁₈H₁₈I₃NO₂) C, H,N.

Example 22

1-(4-Amino-3,5-diiodobenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

A slurry of the isoquinoline 10a (1.94 g, 3 mmol) in MeOH (260 mL) andK₂CO₃ (11.2 g) in H₂O (80 mL) was refluxed for 1 h. MeOH was evaporatedunder reduced pressure, crystals filtered, dried and recrystallized fromEtOAc-hexane to give the title compound (1.39 g, 84%): mp 169-171° C.;¹H NMR (CDCl₃) δ7.55 (s, 2H, ArH), 6.61 (s, 1H, ArH, 6.51 (s, 1H, ArH),4.54 (s, 2H, NH₂), 4.04 (dd, J=9.6, 4.0 Hz, 1H, CH), 3.86 (s, 3H, OMe),3.84 (s, 3H, OMe), 3.18 (m, 1H, CH), 3.03 (dd, J=13.8, 4.0 Hz, 1H, CH),2.92 (ddd, J=12.1, 6.8, 5.2 Hz, 1H, CH), 2.82-2.61 (m, J=13.8, 9.6 Hz,3H, CH); ¹³C NMR (CDCl₃) δ147.51, 147.05, 144.66, 139.97, 132.36,130.14, 127.38, 111.88, 109.28, 81.59, 56.79, 56.01, 55.83, 40.87,40.72, 29.47; IR (KBr) 3416 (NH), 3331 (NH), 1607 (NH bend), 1571, 1512(C═C Ar) cm⁻¹. Anal. (C₁₈H₂₀N₂I₂) C, H, N.

Example 23

6,7-Dihydroxy-1-(3,5-diiodobenzyl)-1,2,3,4-tetrahydroisoquinolineHydrobromide

The isoquinoline 20a (0.19 g, 0.35 mmol) was demethylated using the sameprocedure as 15. Recrystallization from MeOH-ether gave 0.20 g (96%) ofthe title compound: mp 157-159° C. (dec.); ¹H NMR (DMSO-D₆) δ9.13 (bs,1H, OH), 8.88 (bm, 2H, NH+OH), 8.57 (bm, 1H, NH), 8.02 (t, J=1.4 Hz, 1H,ArH), 7.80 (d, J=1.4 Hz, 2H, ArH), 6.61 (s, 1H, ArH), 6.56 (s, 1H, ArH),4.63 (bm, 1H, CH), 3.22-3.41 (m, 2H, CH), 3.14 (m, 1H, CH), 2.71-2.96(m, 3H, CH), ¹³C NMR (CD₃OD) δ147.01 and 145.79 (C-6 and C-7), 145.69(C-4′), 139.18 (C-2′ and C-6′), 141.15 (C-1′), 123.76 and 123.03 (C-4aand C-8a), 116.30 (C-5), 114.21 (C-8), 96.14 (C-3′ and C-5′), 57.25(C-1), 41.02 (C-3), 40.08 (CH₂Ar), 25.60 (C-4); IR (KBr) 3600-2700 (br.OH, NH). 1617, 1521 (C═C Ar) cm⁻¹. Anal. (C₁₆H₁₅Brl₃NO₂) C, H, N.

Example 24

6,7-Dihydroxy-1-(3,4,5-triiodobenzyl)-1,2,3,4-tetrahydroisoquinolineHydrobromide

The isoquinoline 20b (0.23 g, 0.35 mmol) was demethylated using the sameprocedure as 15. Recrystallization from MeOH-ether gave 0.24 g (97%) ofthe title compound: mp 210-213° C. (dec.); ¹H NMR (MeOH-D₄) δ7.92 (s,2H, ArH), 6.63 (s, 1H, ArH), 6.56 (s, 1H, ArH), 4.64 (dd, J=5.7 and 3.1Hz, 1H, CH), 3.3.42-3.53 (m, 1H, CH), 3.2-3.34 (m, 2H, CH), 2.83-3.07(m, 3H, CH), ¹³C NMR (CD₃OD) δ147.11 and 145.90 (C-6 and C-7), 141.06(C-2′ and C-6′), 140.21 (C-1′), 123.70 and 122.98 (C-4a and C-8a),120.90 (C-4′), 116.31 (C-5), 114.14 (C-8), 108.68 (C-3′ and C-5′), 57.04(C-1), 41.01 (C-3), 39.38 (CH₂Ar), 25.62 (C-4); IR (KBr) 3600-2700 (br.OH, NH). 1617, 1540 (C═C Ar) cm⁻¹. Anal. (C₁₆H₁₆Brl₂NO₂) C, H, N.

Example 25

1-(4-Amino-3,5-diiodobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineDihydrochloride

The isoquinoline 20c (1.21 g, 2.2 mmol) was demethylated in the samemanner as 20b to give 1.14 g (76%) of the dihydrobromide salt: mp155-157° C. (dec.). The product was dissolved in MeOH, chromatographed(silica gel, EtOAc-NH₄OH 100:1), evaporated with EtOH (×5). To anethanol solution was added 1N etherial solution of HCl (3 mL),concentrated, precipitated with EtOAc and recrystallized fromMeOH-i-PrOH: mp 176-178° C. (dec.); ¹H NMR (DMSO-D₆) δ9.15 (br s, 1H,OH), 8.89 (br.s, 1H, NH₂ ⁺), 7.68 (s, 2H, H-2′), 6.64 (s, 1H, H-5), 6.55(s, 1H, H-8), 5.06 (br s, 2H, NH₂), 4.47 (m, 1H, H-1), 3.40-2.67 (m, 6H,H-3+H-4+CH₂Ar); ¹³C NMR (CD₃OD) δ147.99 (C-4′), 146.84 and 145.75 (C-6and C-7), 141.60 (C-2′ and C-6′), 128.78 (C-1′), 123.75 and 123.33 (C-4aand C-8a), 116.24 (C-5), 114.16 (C-8), 81.86 (C-3′ and C-5′), 57.59(C-1), 41.07 (C-3), 39.07 (CH₂Ar), 25.68 (C-4); IR (KBr) 3600-2500 (br,OH, NH), 1607 (NH bend), 1529 (C═C Ar) cm⁻¹. Anal.(C₁₆H₁₆I₂N₂O₂.2HCl.H₂O) C, H, N.

Example 26

1-(4-Acetamido-3-iodobenzyl)-6,7-dimethoxy-2-trifluoroacetyl-1,2,3,4-tetrahydroisoquinoline

To a solution of isoquinoline 9a (0.52 g, 1 mmol) in hot benzene (15 mL)was added Ac₂O (0.51 g, 5 mmol). The solution was refluxed for 1 h.Reaction mixture was allowed to cool. A white crystals were filtered.Mother liquor was concentrated and hexane was added. Slightly creamycrystals were filtered, total yield 0.53 g (94%). To get analyticalsample the compound was recrystallized from EtOAc -hexane: mp 174-175°C.; ¹H NMR (CDCl₃) δ8.11 (d, J=8.3 Hz, 1H, H-5′), 7.52 (d, J=1.5 Hz, 1H,H-2′), 7.36 (s, 1H, NH), 7.10 (dd, J=8.3, 1.5 Hz, 1H, ArH), 6.60 (s, 1H,ArH), 6.32 (s, 1H, ArH), 5.23 (t, J=6.6 Hz, CH), 3.94 (m, 1H, CH), 3.87(s, 3-H, OMe), 3,72 (s, 3-H, OMe), 3.54 (ddd, OMe=14.1, 10.4 Hz, 3.8 Hz,1H, CH), 3.06 (m, 2H, CH), 2.90 (ddd, J=15.9 Hz, 10.4 Hz, 5.2 Hz, 1H,CH), 2.68 (dt, J=16.0, 4 Hz, 1H, CH), 2.23 (s, 3H, Ac); ¹³C NMR (CDCl₃)δ168.12, 155.90 (q), 148.30, 147.63, 139.63, 137.12, 134.95, 130.53,126.19, 124.95, 121.73, 116.44 (q), 111.10, 110.17, 89.68, 55.91, 55.33,40.75, 40.50 (q), 28.51, 24.75; IR (KBr) 3395 (NH), 1688 (C═O), 1519(C═C Ar) cm⁻¹. Anal. (C₂₂H₂₂F₃IN₂O₄) C, H, N.

Example 27

1-(4-Acetamido-3-iodobenzyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline

The title compound (0.57 g, 69%) as a glassy solid was obtained from theisoquinoline 22 (0.99 g, 1.76 mmol) in the same manner as 20c. ¹H NMR(CDCl₃) δ8.12 (d, J=8.3 Hz, 1H, H-5′), 7.70 (d, J=1.7 Hz, 1H, ArH), 7.38(s, 1H, NH), 7.26 (dd, J=8.3 Hz, 1.7 Hz, 1H, ArH), 6.63 (s, 1H, ArH),6.60 (s, 1H, ArH), 4.11 (dd, J=9.6 Hz, 3.8, 1H, CH), 3.10-3.25 (m, 2H,CH), 2.92 (m, 1H, CH), 2.63-2.86 (m, 3H, CH₂Ar, CH), 2.25 (s, 3H, Ac);¹³C NMR (CDCl₃) δ168.19, 147.54, 147.05, 139.31, 137.30, 136.66, 130.12,129.92, 127.28, 122.25, 111.85, 109.27, 90.50, 56.64, 55.99, 55.79,41.63, 40.61, 29.30, 24.66; IR (KBr) 3391 (NH), 1676 (C═O), 1515 (C═CAr) cm⁻¹. Anal. (C₂₀H₂₃IN₂O₃) C, H, N.

Example 28

1-(4-Amino-3-iodobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineDihydrochloride

The title compound was obtained in the same manner as 21c from theisoquinoline 23 (0.42 g, 0.90 mmol). The product was recrystallized fromMeOH (twice) to give 0.32 g (64%). The compound was dissolved in NaHCO₃solution and extracted with EtOAc (×5). The solution was dried (MgSO₄)and evaporated. 1M HCl in ether (2 mL) was added to the methanolsolution of the residue. The solution was concentrated and put in arefrigerator. The white crystals were filtered, washed with EtOAc anddried: dec.p. 186-190° C.; ¹H NMR (DMSO-D₆) δ9.05 (bs, 1H, OH), 7.68 (d,J=1.7 Hz, 1H, ArH), 7.16 (dd, J=8.2 Hz, 1.7 Hz, 1H, ArH), 6.94 (d, J=8.2Hz, 1H, ArH), 6.57 (s, 1H, ArH), 6.55 (s, 1H, ArH), 4.46 (m, 1H, CH),3.27 (m, 1H, CH), 3.00-3.20 (m, 2H, CH), 2.80-3.00 (m, 2H, CH), 2.74(dt, J=16.8 Hz, 5.9 Hz, CH); ¹³C NMR (CD₃OD) δ147.00 and 145.76 (C-6 andC-7), 1412.68 (C-2′), 138.21 (C-4′), 136.27 (C-1′), 132.35 (C-6), 123.82and 123.10 (C-4a and C-8a), 116.27 (C-5), 114.33 (C-8), 124.24 (C-5′),91.49 (C-3′), 57.27 (C-1), 40.90 (C-3), 39.87 (CH₂Ar), 25.659 (C-4); IR(KBr) 3600-2300 (br, OH, NH), 1607 (NH bend), 1526 (C═C Ar) cm⁻¹. Anal.(C₁₆H₁₇IN₂O₂.2HCl) C, H, N.

Example 29

1-(4-Acetamido-3-iodobenzyl)-6,7-dibenzyloxy-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline

To a cold solution (0° C.) of isoquinoline 9b (0.68 g, 1 mmol) and Et₃N(0.34 g, 3 mmol) in CH₂Cl₂ (10 mL) was added AcCI (0.16 g, 2 mmol). Thecooling bath was removed and the mixture was stirred overnight. Thesolution was washed with water (2×), dried over MgSO₄, filtered,evaporated. Ether was added and evaporated again to give glassy solid(0.65 g, 90%): mp 62-64° C.; ¹H NMR (CDCl₃) δ(the spectrum consists of 2rotamers of 5:3 ratio) 8.12 and 8.06 (d, J=8.2), 7.59-7.25 (m, 11H,ArH), 7.06 and 6.98 (m, 1H, ArH), 6.70 and 6.65 (s, 1H, ArH), 6.48 and6.35 (s, 1H, ArH), 5.24-4.87 (m, 5H, CH₂O +CH), 4.12 and 3.73 (m, 1H,CH), 3.27-3.11 (m, 1H, CH), 2.98-2.60 (m, 3H, CH₂Ar+CH), 2.60-2.37 (m,1H, CH), 2.22 (s, 3H, Ac), 1.43 and 1.31 (s, 9H, t-Bu); IR (KBr) 3389(NH), 1688 (C═O), 1512 (C═C Ar) cm⁻¹. Anal. (C₃₇H₃₉IN₂O₅) C, H, N.

Example 30

1-(4-Benzoylamino-3-iodobenzyl)-6,7-dibenzyloxy-2-tert-butoxycarbonyl-1,2,3,4-tetrahydroisoquinoline

To a cold solution (0° C.) of isoquinoline 9b (0.68 g, 1 mmol) and Et₃N(0.30 g, 3 mmol) in 10 mL of CH₂Cl₂ was added benzoyl chloride (0.28 g,2 mmol), the cooling bath was removed and the mixture was stirredovernight. CH₂Cl₂ was added (30 mL), the solution was washed with water,dried over MgSO₄, filtered and evaporated till dryness. The oily residuewas dissolved in ether and evaporated to give 0.60 g (76%) of a glassysolid. The compound was purified by column chromatography (silica gel,EtOAc-hexane 1:2): mp 151-153° C.; ¹H NMR (CDCl₃) δ8.42-6.36 (m, 18H,Ar), 5.20-4.90 (m, 5H, 2×CH₂O+H-1), 4.20-2.15 (m, 6H, aliphatic),1.56-1.25 (m, 9H, t-Bu); IR (KBr) 3397 (NH), 1687 (C═O), 1513 (C═C Ar)cm⁻¹. Anal. (C₄₂H₄₁IN₂O₅) C, H, N.

Example 31

1-(4-Acetamido-3-iodobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineHydroiodide

To a solution of isoquinoline 25a (0.40 g, 0.5 mmol) in anhydrous MeCN(5 mL) was added TMSI (0.40 g, 2 mmol) via syringe in argon atmosphere.The solution was stirred for 6 h followed by MeOH (1 mL) was added andstirring continued for 30 min. CH₂Cl₂ (30 mL) was added to reactionmixture and yellow crystals were filtered, yield 0.19 g (67%). Thecompound was dissolved in MeOH, AcOEt was added and the solution wasconcentrated under reduced pressure. The crystals were filtered: dec.p.172-174° C.; ¹H NMR (DMSO-D6) δ9.39 (s, 1H, NH), 8.86 (bs, 1H, OH), 8.50(bs, 1H, OH), 7.90 (d, J=1.7 Hz, 1H, ArH), 7.41 (d, J=8.2 Hz, 1H, ArH),7.35 (dd, J=8.2, 1.7 Hz, 1H, ArH), 6.63 (s, 1H, ArH), 6.56 (s, 1H, ArH),4.63 (m, 1H, CH), 3.43-2.70 (m, 6H, CH), 2.06 (s, 3H, Ac); ¹³C NMR(CD₃OD) δ172.65 (C═O), 146.98 and 145.81(C-6 and C-7), 142.68 (C-2′),140.11 (C-4′), 137.15 (C-1′), 131.30 (C-6′), 129.10 (C-5′), 123.63 and123.27 (C-4a and C-8a), 116.27 (C-5), 114.15 (C-8), 91.49 (C-3′), 57.60(C-1), 41.01 (C-3), 39.98 (CH₂Ar), 25.68 (C-4), 23.09 (COCH₃); IR (KBr)3600-2400 (br, OH, NH), 1655 (C═O), 1624 (NH bend), 1522 (C═C Ar) cm⁻¹;MS m/z (m+): 439. Anal. (C₁₈H₁₉IN₂O₃.HI.0.25 EtOAc) C, H, N.

Example 321-(4-Benzoylamino-3-iodobenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineHydroiodide

To a mixture of isoquinoline 25b (0.16 g, 2 mmol) in MeCN (4 mL) wasadded TMSI (0.16 g, 0.8 mmol) under argon atmosphere and the solutionwas stirred at room temperature for 7 h. MeOH (1 mL) was added, stirredfor 1 h followed by ether (40 mL) was added and the yellow precipitatewas filtered to give 0.10 g (80%) of the product. The compound wasdissolved in MeOH, EtOAc was added and concentrated until the beginningof crystallization: mp 185-188° C. (dec.); ¹H NMR (DMSO-D6) δ9.98 (s,1H, NHCOPh), 9.18 (s, 1H, NH), 8.88 (br, 2H, OH+NH), 8.54 (br, 1H, OH),8.03-7.93 (m, 3H, ArH), 7.64-7.42 (m, 3H, ArH), 7.49 (d, J=8.1 Hz, 1H,ArH), 7.41 (dd, J=8.1, 1.4 Hz, 1H, ArH), 6.65 (s, 1H, ArH), 6.58 (s, 1H,ArH), 3.43-2.70 (m, 6H, CH; IR (KBr) 3500-2700 (br, NH, OH), 1649 (C═O),1518 (C═C Ar) cm⁻¹. Anal. (C₂₃H₂₁IN₂O₃.HI.0.33 EtOAc) C, H, N.

Example 33

1-(3,5-Bis-trifluoromethylbenzyl)-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinolineHydrochloride

The title compound was obtained from 6c in the same manner as 15. Theproduct was converted to the hydrochloride salt and recrystallizationfrom methanol-ether gave the product as white crystals: mp 239-242° C.;¹H NMR (CD₃OD-D₄) δ7.95 (s, 3H, ArH), 6.65 (s, 1H, ArH), 6.44 (s, 1H,ArH), 4.77 (t, J=7.7 Hz), 3.51 (dt, J=6.88, 12.74 Hz), 3.33 (m, 2H, CH),3.0 (m, 2H, CH), ¹³C NMR (CD₃OD) δ147.15 and 145.81 (C-6 and C-7),140.21 (C-1′), 133.21 (C-3′ and C-5′), 131.61 (C-2′ and C-6′), 124.79(CF₃), 123.79 and 122.63 (C-4a and C-8a), 122.58 (C-4′), 116.40 (C-5),114.35 (C-8), 57.11 (C-1), 41.77 (C-3), 40.55 (CH₂Ar), 25.56 (C-4); IR(KBr) 3420 (NH), 1282 (C—O) cm⁻¹; Anal. (C₁₈H₁₆CIF₆NO₂) C, H, N.

Example 34

The compounds of the foregoing examples 1 to 33 were subjected toelemental analysis to further support the structural determinations. Theresults are summarized in Table I:

TABLE I Elemental Analyses Calculated, % Found, % Example C H N FormulaC H N  5a 62.78 5.85 8.13 C₁₈H₂₀N₂O₅ 62.62 5.84 8.05  5c 55.17 4.40 3.22C₂₀H₁₃F₆NO₃ 55.10 4.41 3.20  6a 65.84 6.14 8.53 C₁₈H₂₀N₂O₄ 65.19 6.178.46  6c 51.68 4.55 3.01 C₂₀H₁₉F₆NO₂.HCl.0.5H₂O 51.70 4.53 2.99  7a56.60 4.51 6.60 C₂₀H₁₉F₃N₂O₅ 56.59 4.52 6.66  7b 64.47 6.59 6.54C₂₃H₂₈N₂O₆ 64.57 6.66 6.48  7c 72.40 6.25 4.82 C₃₅H₃₆N₂O₆ 72.32 6.264.79  8a 60.91 5.37 7.10 C₂₀H₂₁F₃BN₂O₃ 60.97 5.39 7.18  8b 69.32 7.597.03 C₂₃H₃₀N₂O₄ 69.21 7.61 7.05  8c 76.34 6.96 5.09 C₃₅H₃₈N₂O₄ 76.226.98 5.03  9a 46.17 3.87 5.38 C₂₀H₂₀F₃IN₂O₃ 46.40 3.90 5.32  9b 52.685.57 5.34 C₂₃H₂₉IN₂O₄ 52.61 5.56 5.25  9c 62.13 5.51 4.14 C₃₅H₃₇IN₂O₄62.05 5.50 4.04 10a 37.18 2.96 4.34 C₂₀H₁₉F₃N₂O₃ 37.45 3.05 4.32 1137.29 2.66 4.35 C₄₀H₃₄F₆I₄N₄O₆ 37.65 2.77 4.34 12 39.44 3.31 5.11C₃₆H₃₄I₄N₄O₄ 39.58 3.30 5.09 13 38.40 3.08 4.07 C₂₂H₂₁F₃I₂N₂O₄ 38.503.27 4.05 14 39.69 4.24 4.21 C₂₀H₂₂I₂N₂O₃.HCl.0.5Et₂O 39.64 3.94 4.44 1534.36 3.25 4.23 C₁₈H₁₈I₂N₂O₃.HBr.0.25Et₂O 34.27 3.34 4.23 16 39.47 3.173.84 C₂₄H₂₃F₃I₂N₂O₅ 39.41 3.18 3.85 18 32.22 2.80 2.29C₁₆H₁₅I₂NO₃.HBr.0.1Et₂O 32.30 2.76 2.33 19a 38.06 2.87 2.22C₂₀H₁₈F₃I₂NO₃ 38.11 2.93 2.21 19b 31.73 2.26 1.85 C₂₀H₁₇F₃I₃NO₃ 31.872.32 1.84 20a 40.40 3.58 2.62 C₁₈H₁₉I₂NO₂ 40.52 3.65 2.59 20b 32.70 2.742.12 C₁₈H₁₈I₃NO₂ 32.58 2.73 2.05 20c 39.30 3.66 5.09 C₁₈H₂₀I₂N₂O₂ 39.563.73 5.00 21a 32.68 2.74 2.38 C₁₆H₁₅I₂NO₂.HBr 32.77 2.78 2.33 21b 26.222.12 1.96 C₁₆H₁₄I₃NO₂.HBr 27.06 2.19 1.91 21c 31.35 3.29 4.57C₁₆H₁₆I₂N₂O₂.2HCl.H₂O 31.49 3.19 4.35 22 48.99 4.11 4.76C₂₂H₂₂F₃IN₂O₄.0.33PhH 49.05 4.10 4.72 23 51.51 4.97 6.01 C₂₀H₂₃IN₂O₃51.73 5.00 5.98 24 40.96 4.08 5.97 C₁₆H₁₇IN₂O₂.2HCl 41.04 4.13 5.94 25a61.84 5.47 3.90 C₃₇H₃₉IN₂O₅ 61.91 5.46 3.94 25b 64.26 5.29 3.59C₄₂H₄₁IN₂O₅ 64.71 5.32 3.67 26a 38.80 3.77 4.76 C₁₈H₁₉IN₂O₃.0.25EtOAc38.65 3.87 4.57 26b 44.44 3.78 4.26 C₂₃H₂₂IN₂O₃.0.33EtOAc 44.68 3.794.40

Thiazolopyridine Derivatives

2-Amino-4-(2-phthalimidoethyl)thiazole Hydrobromide(13). To a solutionof 12 (2.08 g, 7.0 mmol) in acetone (45 ml) was added a solution ofthiourea (0.535 g, 7.0 mmol) in acetone (25 ml) with rapid rate at roomtemperature. Just after the addition was complete, a precipitateappeared, the suspension was stirred overnight at room temperature andfiltered to afford 2.45 g (98.5%) of 13 as a colorless powder: m.p.258-260° C. (dec) (lit. 195° C. (dec starting point)); ¹H NMR (DMSO-d₆),2.82 (t, J=6.3 Hz, 2H), 3.83 (t, J=6.2 Hz, 2H), 6.56 (s, 1H), 7.81-7.88(m, 4H), 9.01 (bs, 2H); IR (KBr) 3214, 3092, 1767, 1721, 1633, 1573,1402 cm⁻¹. Anal. (C₁₃H₁₂N₃O₂SBr): C, H, N.

N-2-(2′-amino-4′-thiazolyl)ethyl-3,4,5-trimethoxyphenylacetamide (17).(a) To a suspension of 3,4,5-trimethoxyphenylacetic acid (4.52 g, 0.02mol) in dry benzene (200 ml) was added dropwise oxalyl chloride (20 ml,0.23 mol) at 0° C. After the addition was complete, the reaction mixturewas stirred at room temperature until a clear solution was obtained(about 1 h). The solution was then heated at reflux for 2.5 h. Thereaction mixture was cooled to room temperature and evaporated to give ayellow oil. It was dissolved in benzene (˜50 ml) and evaporated again(repeated for two more times). 4.9 g (100%) of the acid chloride wasobtained as a viscous yellow oil after dried in vacuo. ¹H NMR (CDCl₃),δ3.83 (s, 3H), 3.84 (s, 6H), 4.05 (s, 2H), 6.45 (s, 2H); IR (neat) 300,2941, 2840, 1799, 1593 cm⁻¹. (b) To a well-stirred suspension of 14 (976mg, 3.2 mmol), NaOH (512 mg, 12.8 mmol) in CHCl₃ (7 ml) and H₂O (5 ml)was added slowly a solution of above-obtained3,4,5-trimethoxyphenylacetyl chloride (784 mg, 3.2 mmol) in CHCl₃ (6 ml)at room temperature. After the addition was complete, the reactionmixture was stirred vigorously at room temperature for 1.5 h. The CHCl₃layer was separated and the H₂O layer was extracted with CHCl₃. Thecombined organics were dried over anhydrous Na₂SO₄, and concentratedunder reduced pressure. The oily residue was dissolved in CHCl₃ (40 ml),and to which HCl (1.0 M solution in dry Et₂O) (10 ml) was added at 0° C.The whole mixture was concentrated, the oily residue was dissolved inH₂O (10 ml). The aqueous solution was washed successively with EtOAc,Et₂O, CHCl₃ and basified with 20% NaOH. The product was extracted withCHCl₃, the combined organics were washed with brine, dried overanhydrous Na₂SO₄ and concentrated, the resulting solid residue wascrystallized from EtOAc to afford 803 mg (71.4%) of 17 as a colorlesscrystal: m.p. 148-149.5° C.; ¹H NMR (CDCl₃, δ2.57 (t, J=6.2 Hz, 2H),3.42 (q, J=5.8 Hz, 2H), 3.46 (s, 2H), 3.79 (s, 3H), 3.80 (s, 6H), 5.16(bs, 2H), 5.96 (s, 1H), 6.43 (s, 2H), 6.50 (bs, 1H); ¹³C NMR (CDCl₃),δ30.64, 38.88, 44.08, 56.11, 60.78, 103.10, 106.78, 130.53, 136.90,150.07, 153.29, 167.89, 170.71; IR (KBr) 3433, 3266, 3080, 2939, 1646,1624, 1590 cm⁻¹. Anal. (C₁₆H₂₁N₃SO₄): C, H, N.

2-Amino-4-(3′,4′,5′-trimethoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridineDihydrochloride (7). A mixture of 17 (70.3 mg, 0.2 mmol) and phosphorusoxychloride (0.27 ml, 2.9 mmol) in CH₃CN (4 ml) was stirred and heatedat reflux for 5 h. After the reaction mixture was cooled andconcentrated under reduced pressure, the residue was dissolved in MeOH(2 ml) and the solution was heated at reflux for 30 min. Afterevaporation, the residue was dissolved in MeOH and evaporated again(repeated three more times). To the stirred solution of the resultingresidue in MeOH (10 ml) was added NaBH₄ (757 mg, 20 mmol) in portionscautiously at 0° C. After the addition was complete, the reactionmixture was stirred overnight at room temperature. After the reactionmixture was evaporated to dryness under reduced pressure, the residuewas dissolved in H₂O (5 ml), cooled with an ice-water bath and wasbasified with 20% NaOH. The basic solution was extracted with EtOAc, thecombined organics were washed with brine, dried over anhydrous Na₂SO₄and concentrated to give a viscous yellow oil. The oily residue wasdissolved in CHCl₃ (5 ml), and to which HCl (1.0 M solution in dry Et₂O)(2 ml) was added at 0° C. The precipitate was filtered off and washedsuccessively with Et₂O, EtOAc, CHCl₃ and crystallized from MeOH-Et₂O toafford 36.5 mg (44.7%) of 7 as a pale yellow powder: m.p. 230-231° C.(dec); ¹H NMR (DMSO-d₆), δ2.71-2.90 (m, 2H), 2.96-3.03 (m, 1H),3.17-3.23 (m, 3H), 3.64 (s, 3H), 3.75 (s, 6H), 4.77 (bs, 1H), 6.67 (s,2H), 8.48 (bs, 1H), 9.68 (bs, 1H), 9.85 (bs, 1H); ¹³C NMR (CD₃OD),δ21.78, 39.79, 41.02, 54.83, 56.84, 61.17, 108.31, 112.94, 130.73,133.85, 139.15, 155.19, 171.53; IR (KBr) 3392, 2940, 2839, 2771, 1632,1593 cm⁻¹. Anal. (C₁₆H₂₃N₃SO₃Cl₂.0.5H₂O): C, H, N.

N-2-(2′-Amino-4′-thiazolyl)ethyl-3,5-diiodo-4-methoxyphenylacet-amide(18). In the same manner as 17, the title compound was prepared from 14(590.3 mg, 1.94 mmol) and 3,5-diiodo-4-methoxyphenylacetyl chloride(844.8 mg, 1.94 mmol) which in turn was obtained by treating itscorresponding acid[36] with oxalyl chloride as described above for3,4,5-trimethoxyphenylacetic acid. Recrystallization from EtOAc gave642.8 mg (61.0%) of 18 as a colorless crystal: m.p. 175-176° C.; ¹H NMR(CD₃OD), δ2.63 (t, J=6.8 Hz, 2H), 3.35 (s, 2H), 3.41 (t, J=6.8 Hz, 2H),3.79 (s, 3H), 6.05 (t, J=0.8 Hz, 1H), 7.72 (s, 2H); ¹³C NMR (CD₃OD),δ31.87, 39.72, 41.80, 61.14, 90.93, 103.35, 137.10, 141.64,149.90,159.38, 171.47, 172.89; IR (KBr) 3431, 3272, 3083, 2933, 1643,1623, 1579, 1524 cm⁻¹. Anal. (C₁₄H₁₅N₃SO₂I₂): C, H, N.

2-Amino-4-(3′,5′-diiodo-4′-methoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridineDihydrochloride (9). In the same manner as 7, the title compound wasprepared from 18 (380.1 mg, 0.7 mmol). After flash column chromatographyon silica gel, eluting with MeOH/CHCl₃ (1:30), 72 mg (19.5%) of the freebase form of the product was obtained as a white solid, it was treatedwith HCl (1.0 M solution in dry Et₂O) to afford 9 as a pale yellowsolid: m.p. 201-203° C. (dec); ¹H NMR (DMSO-d₆), δ2.67-2.77 (m, 2H),3.02-3.11 (m, 2H), 3.15-3.35 (m, 2H), 3.74 (s, 3H), 4.74 (bs, 1H), 7.90(s, 2H), 8.31 (bs, 2H), 9.59 (bs, 1H), 9.79 (bs, 1H); ¹³C NMR, δ22.45,38.02, 41.48, 54.86, 61.21, 91.85, 112.55, 135.12, 135.46, 142.57,160.65, 171.36; IR (KBr) 3421, 2964, 2937, 2775, 1628, 1577 cm⁻¹. Anal.(C₁₄H₁₇N₃SOCl₂I₂): C, H, N.

N-2-(2′-Acetamido4′-thiazolyl)ethyl-3,5-diiodo-4-methoxyphenylacetamide(19). To a stirred suspension of 18 (434.5 mg, 0.8 mmol) in dry CH₃CN(1.8 ml) was added dropwise a solution of acetic anhydride (o.16 ml, 1.7mmol) in dry benzene (0.6 ml). After the addition was complete, thereaction mixture was heated at reflux for 2.5 h. After the reactionmixture was cooled to room temperature and concentrated under reducedpressure to remove solvents completely, H₂O (5 ml) was added to theresidue and the mixture was basified with saturated NaHCO₃ aqueoussolution to pH 7.5-8.0. The solid material was filtered off andcrystallized from CH₃CN to afford 430 mg (91.8%) of 19 as a colorlesscrystal: m.p. 231-232° C.; ¹H NMR(DMSO-d₆), δ2.10 (s, 3H), 2.69 (t,J=7.0 Hz, 2H), 3.29-3.32 (m, 4 H), 3.71 (s, 3H), 6.70 (s, 1H), 7.67 (s,2H), 8.08 (t, J=5.4 Hz, 1H), 12.04 (s, 1H); ¹³C NMR (DMSO-d₆), δ22.45,31.09, 38.17, 40.12, 60.23, 90.94, 107.97, 136.65, 139.93, 148.29,156.96, 157.52, 168.19, 169.32; IR (KBr) 3429, 3273, 3062, 1644, 1554,1537 cm⁻¹. Anal. (C₁₆H₁₇N₃SO₃I₂): C, H, N.

2-Acetamido-4-(3′,5′-diiodo-4′-methoxyphenylmethyl)-4,5,6,7-tetrahydrothiazolo[5,4-c]pyridineMaleate (10). In the same manner as 7, the title compound was preparedfrom 19 (300 mg, 0.51 mmol). After flash column chromatography on silicagel, eluting with acetone/hexane (1:3), 150 mg (51.7%) of the free baseform of 10 was obtained as a white powder: m.p. 170-172° C.; ¹H NMR(DMSO-d₆), δ2.09 (s, 3H), 2.53-2.60 (m, 2H), 2.66-2.73 (m, 1H),2.77-2.86 (m, 1H), 2.89-2.95 (m, 1H), 3.09-3.15 (m, 1H), 3.72 (s, 3H),4.12-4.13 (m, 1H), 7.80 (s, 2H), 11.91 (bs, 1H); ¹³C NMR (DMSO-d₆),δ22.45, 27.03, 40.41, 40.82, 53.87, 60.22, 90.86, 124.18, 139.29,140.43, 143.70, 155.49, 156.72, 167.99; IR (KBr) 3428, 3252, 2914, 1675,1636, 1565. Anal. (C₁₆H₁₇N₃SO₂I₂): C, H, N. 10 was obtained as a whitepowder by treating the above-obtained free base with maleic acid inCH₃CN: m.p. 121° C. (dec); ¹H NMR (CD₃OD), δ2.18 (s, 3H), 2.93-3.09 (m,4H), 3.38-3.44 (m, 1H), 3.63-3.71 (m, 1H), 4.93-4.96 (m, 1H), 6.26 (s,8/3H), 7.85 (s, 2H); ¹³C NMR (DMSO-d₆), δ22.40, 23.37, 37.73, 40.42,53.73, 60.26, 91.59, 118.22, 134.71, 135.43, 140.67, 142.07, 157.45,157.78, 167.07, 168.60; IR (KBr) 3436, 3049, 2968, 2946, 1700, 1686,1624, 1571 cm⁻¹. Anal. (C₁₆H₁₇N₃SO₂I₂.4/3C₄H₄O₄.1/3Et₂O): C, H, N.

2-Amino-5-(2-phthalimidoethyl)thiazole Hydrobromide (27). In the samemanner as 13, the title compound was prepared from thiourea (2.75 g,36.1 mmol) and 26³² (crude, 10.69 g, 36.1 mmol). Recrystallization fromMeOH/EtOH (1:10) gave 6.19 g (46% based on aldehyde 25³²) of 27 ascolorless plates: m.p. 244-246° C. (dec) (lit.³² 180° C. (dec startingpoint)); ¹H NMR (DMSO-d₆), δ2.96 (t, J=6.2 Hz, 2H), 3.77 (t, J=6.3 Hz,2H), 7.08 (s, 1H), 7.82-7.89 (m, 4H), 9.01 (bs, 2H); IR (KBr) 3308,3222, 3108, 2975, 1764, 1711, 1618, 1608, 1554, 1402 cm⁻¹. Anal.(C₁₃H₁₂N₃O₂SBr): C, H, N.

N-2-(2′-Amino-5′-thiazolyl)ethyl-3,4,5-trimethoxyphenylacetamide (21),In the same manner as 17, the title compound was prepared from 20³²(1.95 g, 6.4 mmol) and 3,4,5-trimethoxyphenylacetyl chloride (1.57 g,6.4 mmol). Recrystallization from CHCl₃/hexanes gave 1.42 g (63.3%) of21 as colorless crystals: m.p. 121-122° C.; ¹H NMR (CDCl₃), δ2.74 (t,J=6.0 Hz, 2H), 3.34 (q, J=6.3 Hz, 2H), 3.43 (s, 2H), 3.79 (d, 9H), 5.22(bs, 2H), 5.78 (t, J=5.6 Hz, 1H), 6.39 (s, 2H), 6.59 (s, 1H); ¹³C NMR(CDCl₃), δ26.84, 40.39, 43.99, 56.07, 60.78, 106.35, 124.42, 130.29,135.80, 137.09, 153.48, 167.34, 170.90; IR (KBr) 3294, 3114, 2995, 2936,1654, 1636, 1588 cm⁻¹. Anal. (C₁₆H₂₁N₃SO₄): C, H, N.

N-2-(2′-Amino-5′-thiazolyl)ethyl-3,4,5-trimethoxyphenethylamineDihydrochloride (24). To a suspension of 21(176 mg, 0.5 mmol) in dry THF(0.5 ml) was added dropwise slowly BH₃.THF(1.0 M in THF, 3.5 ml). Afterthe addition was complete, the reaction mixture was stirred at roomtemperature for 30 min, and then was heated at reflux for 1 h. Thereaction mixture was cooled to room temperature and treated cautiouslywith 10% HCl aqueous solution (3 ml), and the solution was heated atreflux for 30 min. After removal of THF, H₂O (10 ml) was added to theresidue. The acidic solution was basified with 10% NaOH aqueous solutionat 0° C. The product was extracted with CHCl₃ (20, 20, 10 ml), thecombined organic was washed with brine (20 ml), and dried over anhydrousNa₂SO₄. After filtration and evaporation, a viscous oil was obtained, itwas dissolved in CHCl₃ (8 ml) and was treated with HCl (1.0 M in dryEt₂O). The whole mixture was evaporated to dryness and the resultingwhite solid was crystallized in MeOH/Et₂O to give 109 mg (53.1%) of 24as white crystals: m.p. 235° C. (dec); ¹H NMR (CD₃OD), δ2.98-3.03 (m,2H), 3.11-3.16 (m, 2H), 3.29-3.34(m, 4H), 3.72 (s, 3H), 3.84 (s, 6H),6.63 (s, 2H), 7.18 (s, 1H); ¹³C NMR (CD₃OD), δ24.63, 33.53, 48.38,50.25, 56.73, 61.07, 107.24, 121.73, 125.27, 133.76, 138.28, 154.87,172.01; IR (KBr) 3427, 2947, 2767, 1630, 1590 cm⁻¹. Anal.(C₁₆H₂₅N₃SO₃Cl₂): C, H, N.

Radoiligand Binding Studies with β₁ Adrenoreceptors, β₂ Adrenoreceptorsand β₃-Adrenoreceptors Expressed in CHO Cells

Competitive and comparative binding experiments on β₁Adrenoreceptors,.β₂ Adrenoreceptors and β₃-Adrenoreceptors expressed inCHO cells were performed as described previously. Fraundorfer, P. F.;Fertel, R. H.; Miller, D. D.; Feller, D. R. “Biochemical andpharmacological characterization of high-affinity trimetoquinol analogson guinea pig and human beta adrenergic receptor subtypes: evidence forpartial agonism.” J Pharmacol Exp Ther 1994, 270, 665-74. (“FraundorferII”, supra) CHO cells expressing human β₁ Adrenoreceptors, β₂Adrenoreceptors and β₃-Adrenoreceptors (provided by A. D. Strosberg,Institut Cochin de Genetique Moleculaire, Paris, France; and DavidBylund, University of Nebraska, Omaha, Nebr.; respectively) werecultured in Ham's F-12 medium supplemented with 10% fetal bovine serum,50 U/mL-50 μg/mL of penicillin-streptomycin, 2 mM L-glutamine and 50μg/mL of Geneticin in a humidified atmosphere of 5% CO₂-95% air. CHOcells grown to a confluence in 150-mL flasks were detached into Ham'sF-12 medium after treatment with 0.05% trypsin-0.53 mM EDTA solution.The cells were then pelleted and washed three times with Tris-EDTAbuffer (50 mM Tris-HCl, 150 mM NaCl, 20 mM EDTA, pH 7.4) and resuspendedin the same buffer.

Data are expressed as the means±SE of the given number of experiments.All concentration-response and competition binding curves were analyzedusing GraphPad Prism (GraphPad Software, San Diego, Calif., USA).pK_(act) values are expressed relative to the maximal effect for eachcompound or effect at the highest concentration tested (for compoundswith limited solubility). Relative efficacies (e_(π)) were calculatedfrom plots of fractional percent occupancy versus response (% increasein cAMP accumulation) as described by Furchgott and Bursztyn (1967). Therelative efficacies are expressed relative to (−)-isoproterenol, areference β-adrenoceptor agonist.

Competition binding experiments were performed in duplicates using thesewhole cells. Aliquots (150 μL) of cells were added to tubes containing50 μL of [¹²⁵I]ICYP (1.5-5×10⁴ cells/20-60 pM of ICYP) and varyingconcentrations of competing drugs. The final volume in each tube was0.25 mL. Nonspecific binding (5-30%) was determined in the presence of 1μM (±)-propranolol. Incubations were carried out for 60 min at 37° C.Binding reactions were terminated by rapid filtration through WhatmanGF/B glass fiber filters on a Brandel model 12-R tissue harvester.Filters were washed twice with ice cold Tris-EDTA buffer to remove freeICYP. The filters were dried under tissue harvester vacuum andradioactivity was measured by gamma scintillation spectrometry (Beckmanmodel 8000 gamma counter, Palo Alto, Calif.). Specific binding to βAdrenoreceptor sites in these cells varied from 94 to 100%

Thromboxane A₂/Prostaglandin H₂ (TP) Receptor Sites in Human Platelets

For binding experiments, human platelet rich plasma (PRP) wascentrifuged and re-suspended in 50 mM Tris-saline buffer, pH 7.4. Shin,Y.; Romstedt, K. J.; Miller, D. D.; Feller, D. R. “Interactions ofnonprostanoid trimetoquinol analogs with thromboxane A₂/prostaglandin H₂receptors in human platelets, rat vascular endothelial cells and ratvascular smooth muscle cells.” J Pharmacol Exp Ther 1993, 267, 1017-23.Platelets were incubated with 5 nM [³H]SQ 29,548 in a final vol of 0.5mL as described by Hedberg, A.; Hall, S.; Ogletree, M.; Harris, D.; Liu,E. “Characterization of [5-6³H]SQ 29,548 as a high affinity ligand forthromboxane A₂/prostaglandin H₂ receptors in human platelets”. J.Pharmacol. Exp. Ther. 1988, 245, 786-792. Unlabelled SQ 29,548 (50 μM)was used to determine nonspecific binding. Varying concentrations ofeach competing drug were used to quantify the inhibition of specific[³H]SQ 29,548 binding. Samples were incubated 30 min at roomtemperature, and rapidly filtered by vacuum through Whatman GF/C glassfiber filters on a Brandel cell harvester and washed for 10 sec with icecold TRIS-saline buffer. Filters were placed in plastic scintillationvials containing 10 mL of an emulsion-type scintillation mixture andradioactivity measured by liquid scintillation spectrometry. Specificbinding to human platelets varied between 88 to 95%.

Competitive binding data were analyzed using the PC-version of theradioligand binding program LIGAND (McPherson, 1985). Inhibitoryconcentration-50 (IC₅₀) value of each competing drug was determinedgraphically from individual plots of percent radioligand bound versuslog drug concentration on β-adrenoceptors and human platelets. Accordingto the reported method (Cheng, Y.; Prusoff, W. H. Relationship betweenthe inhibition constant (K_(i)) and the concentration of the inhibitorwhich causes 50 percent inhibition (I₅₀) of an enzymatic reaction,Biochem. Pharmacol. 1973, 22, 3099-3108), K_(i) values were calculatedfrom the obtained IC₅₀ values. Dissociation constants (K_(i)) for eachcompeting drug were calculated using the equation:$K_{i} = \frac{I\quad C_{50}}{\left( {1 + \frac{L}{K_{L}}} \right)}$

and the data expressed as pK_(i) (i.e., −log K_(i)) values. The K_(L)values used in the above equation are 17 pM, for β₁ Adrenoreceptor; 10pM for β₂ Adrenoreceptor; 11 pM for β₃-Adrenoreceptor; and 3.1 nM forThromboxane A₂/Prostaglandin H₂ receptors, respectively.

cAMP Radioimmunoassay (cAMP-RIA Assay). Chinese hamster ovary (CHO)cells expressing either human β₁-, β₂- or β₃-adrenoceptor (AR) subtypeswere used as previously described (Fraundorfer, P. F.; Lezama, E. J.;Salazar-Bookaman, M. M.; Fertel, R. H.; Miller, D. D.; Feller, D. R.Isomeric-activity ratios of trimetoquinol enantiomers on β-adrenergicreceptor subtypes: functional and biochemical studies, Chirality 1994,6, 76-85). These cells were grown to confluence in 60 mm dishes, washedwith Hank's balanced salt solution, and then incubated with Hank'sbalanced salt solution (pH 7.4) containing 20 mM HEPES and 1 mM3-isobutyl-1-methylxanthine (IBMX) and 1 mM L-ascorbic acid for 30 minat 37° C. Varying concentrations (10⁻¹¹ to 10⁻⁴ M) of the drugs wereadded with an additional 30 min of incubation. After removal of theHank's buffer, the cAMP generated within the cells was extracted by theaddition of trichloroacetic acid (6% w/v). cAMP content was determinedas the amount of [¹²⁵I]-labeled succinyl-cAMP tyrosine methylester/antibody precipitated, as described by Brooker et al. (Brooker,G.; Harper, J. F.; Terasaki, W. L.; Moylan, R. D. Radioimmunoassay ofcyclic AMP and cyclic GMP. In Advances in Cyclic Nucleotide Research;Brooker, G., Greengard, P. and Robinson, A., Ed.; Raven Press: New York,1979, pp 1-33). The precipitated protein was dissolved in 0.1N NaOH.Protein content was determined by the method of Lowry et al. (Lowry, O.H.; Rosebrough, N. J.; Farr, A. L.; Randall, R. J. Protein measurementwith the Folin phenol reagent., J. Biol. Chem. 1951, 193, 265-275),using bovine serum albumin as the standard. Data are expressed as themeans±SE of the given number of experiments. All concentration-responseand competition binding curves were analyzed using GraphPad Prism(GraphPad Software, San Diego, Calif., USA). pK_(act) values areexpressed relative to the maximal effect for each compound or effect atthe highest concentration tested (for compounds with limitedsolubility). Relative efficacies (e_(π)) were calculated from plots offractional percent occupancy versus response (% increase in cAMPaccumulation) as described by Furchgott and Bursztyn (Furchgott, R. F.,and Bursztyn, P. “Comparison of dissociation constants and relativeefficacies of selected agonists on parasympathetic receptors” Ann. N.Y.Acad. Sci. 1967, 882-889).

cAMP response element (CRE)-luciferase(LUC) reporter gene (CRE-LUC)assay. CHO cells stably expressing human β₁-, β₂-, or β₃-AR subtypeswere transfected with a 6 CRE-LUC plasmid (gift from Dr. A. Himmler,Vienna, Austria) using electroporation with a single 70 ms, 150V pulse(Vansal, S. S.; Feller, D. R. Development of a rapid and efficientcyclic AMP assay for evaluating β-adrenergic receptor ligands.,Naunyn-Schmiedeberg's Arch. Pharmacol. Suppl. 2 1998, 258, R659). Thetransfected CHO cells were seeded at a density of 40,000/well in 96 wellmicrotiter plates (Culturplate, Packard) and allowed to grow for 20hours. After 20 hours, the cells were treated with varying drugconcentrations (10⁻¹¹ to 10⁻⁴ M) for 4 hours. Following drug exposures,the cells were lysed and luciferase activity measured using the LucLite®assay kit (Packard). Changes in light production were measured by aTopcount® luminometer (Packard).

Functional Activity of TMQ Analogs in Isolated Rat Tissues

Male Sprague Dawley rats (Harlan Industries, Cumberland, Ind.) housedunder a 12 hour light/dark cycle and fed Purina Rodent Laboratory Chow(Ralston Purina., St. Louis, Mo.) and water ad libitum, were used forthe studies. On the day of the experiment, the rats weighting 200-430 gwere killed by cervical dislocation and tissues were quickly removedaccording to standard procedures (Staff of the Department ofPharmacology, University of Edinburg, in Pharmacological Experiments onIsolated Preparations, p. 104. Livingstone, London, 1968). Chronotopicresponses of spontaneously beating right atria were used as a model formeasuring β₁-AR mediated activity (Konkar, A. A., Fraundorfer, P. F.,Fertel, R. H., Burkman, A. M., Miller, D. D., and Feller, D. R.“Pharmacological Activities of trimetoquinol and 1-benzylhalogen-substituted analogues on rat β-adrenoceptor subtypes. Eur. J.Pharmacol. 1996, 305, 63-71). Relaxations of spirally cut trachealstrips precontracted with 3×10⁻⁷M carbachol, and of longitudinalsegments of the esophageal smooth muscle precontracted with 10⁻⁶Mcarbachol (in the presence of 1 μM pindolol and 10 μM phentolamine),were used to measure β₂-and β₃-AR-mediated activity, respectively(Konkar, A. A., Fraundorfer, P. F., Fertel, R. H., Burkman, A. M.,Miller, D. D., and Feller, D. R. “Pharmacological Activities oftrimetoquinol and 1-benzyl halogen-substituted analogues on ratβ-adrenoceptor subtypes. Eur. J. Pharmacol. 1996, 305, 63-71; Lezama, E.J., Konkar, A. A., Salazaar-Bookaman, M. M., Miller, D. D., and Feller,D. R. “Pharmacological study of atypical β-adrenoceptors in ratesophageal smooth muscle. Eur. J. Pharmacol., 1996, 308, 69-80).Contractions of spirally cut aortal strips and inhibition ofphenylephrine-induced contraction of the tissue, were used to measureα-AR mediated agonist or antagonist activity of the compoundsrespectively. The tissues were isolated and prepared for measurement offunctional activity as per protocols described earlier (Konkar, A. A.,Fraundorfer, P. F., Fertel, R. H., Burkman, A. M., Miller, D. D., andFeller, D. R. “Pharmacological Activities of trimetoquinol and 1-benzylhalogen-substituted analogues on rat β-adrenoceptor subtypes. Eur. J.Pharmacol. 1996, 305, 63-71; Staff of the Department of Pharmacology,University of Edinburg, in Pharmacological Experiments on IsolatedPreparations, p. 104. Livingstone, London, 1968). All tissues weresuspended and equilibrated in modified Kreb's buffer in water-jacketedbaths at 37° C. Resting tensions of 1 g for right atria, trachea andaorta, and of 200 mg for esophageal smooth muscle were used. All tissueresponses were measured on a Grass Polygraph Model 7C with a GrassFT-03C isometric force-displacement transducer. Cumulative concentrationresponse curves for each drug were constructed by the method of vanRossum (van Rossum, J. M. “Cumulative dose-response curves. II.Technique for making of dose-response curves in isolated organs and theevaluation of drug parameters. Arch. Int. Pharmacodyn. 1963, 143,299-300). Increasing concentrations of compounds were added every 2-3min with

(−)-isoproterenol and every 10-15 min with TMQ analogs, or until nofurther change in response was observed.

In the right atrium, the concentration response curve for(−)-isoproterenol was followed by complete washout of the drug, afterwhich a curve for either acetamido- or chloroacetamido DITMQ wasconstructed. The tissue was again washed 6-7 times with 10 ml of buffer,followed by repeated washes every 10-15 min. Changes observed in theduration of chronotropic effect following repeated washes was used as anindicator of ‘irreversible’ binding of the compound to the atrialtissue. A second concentration response curve with (−)-isoproterenol wasconstructed in atria to determine desensitization effects.

The concentration response curves in trachea and esophagus culminatedwith a final concentration of 10⁻⁵M(−)-isoproterenol, to determine themaximal relations induced in the tissue and express functional responsesof the TMQ analogs as a percentage of maximal

(−)-isoproterenol-induced response. Carbachol-precontracted tissues wereincluded as controls through the duration of relaxation studies.

Studies with aorta were performed in the presence of 1 μm pindolol, toblock β-AR-mediated effects. Concentration response curves tophenylephrine were followed by washout of the drug 30 min incubationwith 10⁻⁵ M acetamido- or chloroacetamido-DITMQ. A second phenylephrineconcentration-response was then constructed to determine any α-ARblocking activity of the TMQ analogs. In control experiments, secondconcentration response curves of phenylephrine were constructed in theabsence of treatment with the compounds.

TABLE 1 Human β₂-Adrenoceptor Expressed in CHO Cells and PlateletThromboxane A₂/Prostaglandin (TP) Receptor Binding Affinities ofTrimetoquinol (TMQ) Analogs.

Human β₂ Adrenoreceptor Human TP 1-Benzyl Substituents CHO^(a)receptors^(b) Compnd R₁ R₂ R₃ pKi ± SEM P.R.^(c) pKi ± SEM P.R.^(c)  1OCH₃ OCH₃ OCH₃ 7.36 ± 0.23 1.0 6.79 ± 0.09 1.00  2 I OCH₃ I 8.69 ± 0.1621 7.33 ± 0.07 3.5 21c I NH₂ I 8.81 ± 0.15 28 6.73 ± 0.12 0.87 24 I NH₂H 8.19 ± 0.27 6.8 6.00 ± 0.02 0.16 15 I NHCOCH₃ I 8.06 ± 0.13 5.0 6.45 ±0.11 0.46 26a I NHCOCH₃ H 8.11 ± 0.16 5.6 5.83 ± 0.14 0.11 21a I H I9.52 ± 0.13 150 6.75 ± 0.07 0.91 21b I I I 8.82 ± 0.18 29 4.22 ± 0.030.003 26b I NHCOPh H 8.70 ± 0.03 22 5.27 ± 0.13 0.03 18 I OH I 7.93 ±0.03 3.7 4.72 ± 0.09 0.009 27 CF₃ H CF₃ 5.36 ± 0.32 0.01 4.08 ± 0.020.002 ^(a)Using [¹²⁵I] ICYP as radioligand, N = 4-9 ^(b)Using [³H] SQ29,548 as radioligand, N = 4-9 ^(c)PR = potency ratio relative to cmpd.1 (TMQ). PR = antilog [pKi(drug)-pKi(TMQ)]

TABLE 2 Selectivity of Trimetoquinol (TMQ) Analogs for Human β₂-andβ₁-Adrenoceptors Expressed in CHO cells pKi ± SEM Compound human β₁CHO^(a) human β₂ CHO^(a) β₂/β₁ selectivity^(b) 1 6.49 ± 0.06 7.36 ± 0.237.4 2 7.10 ± 0.06 8.69 ± 0.16 39 21a 6.74 ± 0.30 9.52 ± 0.13 600^(a)using [125|] ICYP as radioligand for β₁-and β₂ Adrenoreceptorexpressed in CHO cells, N = 4-9 bβ₂/β₁-selectivity = Ki (β₁Adrenoreceptor)/Ki (β₂ Adrenoreceptor)

TABLE 3 Agonist Activities of (−)-Isoproterenol, AcetamidolDITMQ andChloracetamido- DITMQ on β-Adrenoceptors in Isolated Rat Tissues. RightAtria Esophageal Smooth (β-AR) Trachea Muscle (Atypical-β/β₃-AR)(−)Isoproterenol pEC₅₀ 8.95 ± 0.06 8.00 ± 0.05 7.34 ± 0.08 I.A. 1.001.00 1.00 (n) (5) (8) (12) AcetamidoDITMQ (A-14) pEC₅₀ 8.96 ± 0.04  9.22± 0.07† 8.68 ± 0.12 I.A. 0.93 ± 0.04  0.84 ± 0.02†  0.99 ± 0.03t (n) (4)(4) (7) ChloroacetamidoDITMQ (A-37) pEC₅₀ 8.94 ± 0.07  8.90 ± 0.05† 8.08 ± 0.03† I.A.  0.81 ± 0.05†  0.83 ± 0.02†  0.99 ± 0.01† (n) (4) (4)(6) Data are calculated as pEC₅₀ (−log EC₅₀, concentration required toproduce a response equal to 50% of maximal response elected by the drug)and I.A. (Intrinsic activity, maximal drug-induced response relative tothe maximal response elicited by (−)-isoproterenol). The values are mean± SEM of the number of experiments indicated in parentheses. † Indicatessignificant difference in value of TMQ analog compared to correspondingvalue of (−)-isoproterenol (P < 0.05).

TABLE 4 COMPOUND p_(K) _(i) Pk_(act) E_(max) (−)Isoproterenol 4.45 ±0.06 (14) 7.90 ± 0.12 (16) 100 BRL 37344 6.96 ± 0.08 (5) † 8.90 ± 0.12(9) † 103.3 ± 6.80  S(−)TMQ 5.67 ± 0.03 (5) † 8.19 ± 0.19 (7) 87.65 ±6.90  (±)TMQ 5.11 ± 0.12 (8) † 8.69 ± 0.14 (10) † 125.3 ± 9.20  DITMQ(A-11) 6.34 ± 0.03 (5) † 9.40 ± 0.08 (9) † 96.90 ± 10.10 AminoDITMQ(A-35) 6.14 ± 0.08 (5) † nd nd AcetamidoDITMQ (A-14) 7.28 ± 0.06 (5) †9.34 ± 0.12 (6) † 89.57 ± 6.93  ChloroacetamidoDITMQ (A-37) 6.49 ± 0.05(5) † 9.05 ± 0.16 (6) † 92.48 ± 6.59  BromoacetamidoDlTMQ (A-38) 6.70 ±0.05 (6) † 9.36 ± 0.39 (5) † 87.27 ± 12.21 6,7-Dimethoxy-acetamidoDITMQ4.84 ± 0.03 (5) † nd nd 6,7-Dimethoxy TMQ 3.88 ± 0.07 (4) † no activityup to 3 × 10⁻⁵ M M 6,7-Methylenedioxy TMQ 4.29 ± 0.05 (5) 5.92 ± 0.12(8) † 70.90 ± 4.41†* DemethoxyDITMQ 5.80 ± 0.03 (5) † 8.74 ± 0.10 (4) †97.69 ± 5.85 IsothiocyanatolTMQ (A-46) 5.83 ± 0.12 (4) † 8.61 ± 0.15 (4)† 104.1 ± 7.10 Inhibition constants (-log K_(i) or pK_(i)) for bindingand functional activity constants (-log EC₅₀ or pK_(act)) for cAMPaccumulation in CHO cells expressing rat-β₃-AR. E_(max) is the maximalcAMP accumulation stimulated by the compounds relative to that of(−)-isoproterenol. Values are mean ± SEM of the number of experimentsindicated in parentheses. nd = value not determined. †Indicatessignificant difference in value of TMQ analog compared to correspondingto value of (−)-isoproterenol (P < 0.05).

TABLE 5 Human β3-Adrenoceptors Binding Affinities of TMQ Analogs pK, ±SEM^(a) Human β₁-AR Human β₂-AR Human β₃-AR ISO 5.80 ± 0.07 6.17 ± 0.124.73 ± 0.25 TMQ 6.49 ± 0.06 7.36 ± 0.23 5.43 ± 0.28 8 (A-11) 7.10 ± 0.068.69 ± 0.16 7.67 ± 0.24 7 (B-29) 5.21 ± 0.08 6.21 ± 0.12 4.17 ± 0.05 9(B-28) 6.14 ± 0.08 6.37 ± 0.08 5.83 ± 0.15 ^(a)Human β₁-β₂- and β₃-ARwere expressed in CHO cells. [¹²⁵|] ICYP was used as the radioligand.K_(i) values were calculated using the following equation: K_(i) (nM) =IC₅₀ (1 + [L]/K_(d)), wherein IC₅₀ is the concentration (nM) of ananalog at which the radioligand binding was reduced by 50%; [L] is theradioligand concentration used; K_(d) is the radioligand equilibriumdissociation constant. pK_(i) = −logK_(i); SEM = standard error of mean.N = 3-9.

TABLE 6 Human β-Adrenoceptors (AR) Functional Activities of TMQ AnalogsHuman β₁-AR Human β₂-AR Human β₃-AR pK_(act) ± SEM^(a) I.A. ± SEM^(b)pK_(act) ± SEM I.A. ± SEM pK_(act) ± SEM A. cAMP-RIA ASSAY^(c) Iso 8.75± 0.14 100 84.0 ± 0.17 100 7.37 ± 0.11 100 TMQ 8.70 ± 0.11 109 ± 10 8.33± 0.24^(d) 95 ± 3 8.60 ± 0.15  95 ± 3 8 (A- 8.11 ± 0.13 103 ± 4 8.47 ±0.12 56 ± 9 8.76 ± 0.2 120 ± 9 11) 7 (B- N.A.^(e) <10 N.A. 20 ± 1 5.06 ±0.01  54 ± 1 29) 9 (B- N.A.  <5 N.A.  <5 6.95 ± 0.11  67 ± 3 28) 10 N.A.<10 N.A. <10 N.A. <10 B. CRE-LUC assay^(c) 9 (B- N.A. <10 N.A. <15 6.71± 0.18  62 ± 3 28) 24 N.B. <10 N.A. <10 N.A. <10 ^(a)Human β₁-, β₂- andβ₃-AR were expressed in CHO cells. K_(act) is the molar drugconcentration which produces a cAMP response equal to 50% of its maximalresponse, pK_(act) = −logK_(act). ^(b)I.A. = Intrinsic Activity,expressed as the percentage of a maximal analog response relative to themaximal response (100%) of R-(−)-isoproterenol (ISO). ^(c)seeExperimental Section. ^(d)Data is for S-(−)-TMQ isomer. ^(e)N.A. '2 Notactive at 100 μM. Values are the mean ± SEM of N '2 4-12.

TABLE 7 Data on TMQ analogs using the CRE-LUC assay β₁-AR β₂-AR β₃-ARpK_(act) ± SEM pk_(act) ± SEM pK_(act) ± SEM Compound (n) I.A. (n) I.A.(n) I.A. 6-Monophenolic TMQ 5.71 ± 0.13 58 6.64 ± 0.15 38 7.45 ± 0.09 90analog (A-4) (8) (8) (8) Non-catechol TMQ N.D. 22 N.D. 21 7.54 ± 0.22 62Analog (A-3) (8) (8) (8) Agonist potencies (pKact values) and intrinsicactivities (IA) of noncatechol (A3) and 6-monophenolic (A4) analogs forhuman β-adrenoceptor subtypes expressed in Chinese hamster ovary cells.IA values are expressed relative to the maximal response to(−)-isoproterenol in these CHO cell systems expressing the three humanβ-adrenoceptor subtypes. Agonist activities were measured using thecyclic AMP response element-luciferase reporter gene (CRE-LUC) assay.

TABLE 8 Selectivity of TMQ Analogs for Human β₁, β₂, and β₃Adrenoreceptors Expressed in CHO Cells and Functional Activities of TMQAnalogs in CHO Cells Expressing Human β₃ Adrenoreceptors. hβ₃ cAMPMOLECULAR EC₅₀ (nM) +/− hβ₃ cAMP hβ₁ Binding hβ₂ Binding STRUCTURE SEM %Iso +/− SEM KI (nM) ki (nM)

506 +/− 137 32.3 +/− 5   8400 +/− 8100 534 +/− 67 

45 +/− 9  81 +/− 3  14.2 +/− 9.8  24 +/− 9 

<4 119 +/− 6   25 +/− 1.3 3.1 +/− 1.7

<4 108 +/− 2  63.4 +/− 0.9 

>3160 >3000 >3000

33.5 +/− 7   89 +/− 5  278 +/− 59   47 +/− 4.3

>1 100 +/− 2  6.7 +/− 1.3 6.5 +/− 1.5

Conclusion

The invention has been described herein with regard to particularpreferred operating circumstances and requirements, and in a particularcontext. Those of ordinary skill will clearly understand the applicationof the invention and its uses in other diverse circumstances and will,with the guidance provided herein, be able to adapt the invention to theparticular requirements of other contexts of practice of the invention.

The foregoing description and disclosure of the present invention isintended to be illustrative for the guidance of those of ordinary skillin the art to which the invention pertains, and is not intended todefine or limit the scope of the invention. The scope of the inventionis defined and limited only in the appended claims.

What is claimed is:
 1. A compound having the structure:

wherein: R₁ and R₃ are independently selected from the group consistingof hydrogen, halogen, alkyl, aryl alkyl, CF₃, and OCH₃; R₂ is selectedfrom the group consisting of hydrogen, halogen, OH, OCH₃, OCH₂COOH,C(O)-aryl, NCS, NH₂, N₃, NHR₈, NHCH₂COOH, NHCOR₁₃, NHCONHR₁₃, andNHCOSR₁₃; R₄ and R₅ are each independently selected from the groupconsisting of hydrogen, OH, and halogen; R₆ and R₇ are eachindependently selected from the group consisting of hydrogen andhalogen; R₈ is selected from the group consisting of hydrogen, loweralkyl of from 1 to 8 carbons, halogen, OCH₃, and CF₃; and R₁₃ isselected from the group consisting of hydrogen, lower alkyl of from 1 to8 carbons, phenyl, halogen, OCH₃, CF₃, and —CH₂R′, wherein R′ ishalogen; wherein no more than one of R₁, R₂, and R₃ is OCH₃ or hydrogenand one, but not both, of R₄ and R₅ is OH; or a pharmaceuticallyacceptable salt thereof.
 2. The compound of claim 1, wherein R₄ is OHand R₅ is hydrogen or halogen.
 3. The compound of claim 1, wherein R₅ isOH and R₄ is hydrogen or halogen.
 4. The compound of claim 1, wherein R₆and R₇ are each halogen.
 5. The compound of claim 1, wherein R₆ and R₇are each hydrogen.
 6. The compound of claim 1, wherein R₂ is OCH₃, NH₂,or NHCOR₁₃.
 7. The compound of claim 1, wherein R₁ and R₃ are halogen.8. The compound of claim 1, wherein R₁ is halogen, R₂ is OCH₃ or NH₂,and R₃ is hydrogen.
 9. The compound of claim 1, wherein R₅ is OH, R₄ ishydrogen or halogen, R₂ is OCH₃, NH₂, or NHCOR₁₃, and R₁ and R₃ arehalogen.
 10. A pharmaceutical composition, comprising a pharmaceuticallyacceptable carrier and at least one compound having the structure:

wherein: R₁ and R₃ are independently selected from the group consistingof hydrogen, halogen, alkyl, aryl alkyl, CF₃, and OCH₃; R₂ is selectedfrom the group consisting of hydrogen, halogen, OH, OCH₃, OCH₂COOH,C(O)-aryl, NCS, NH₂, N₃, NHR₈, NHCH₂COOH, NHCOR₁₃, NHCONHR₁₃, andNHCOSR₁₃; R₄ and R₅ are each independently selected from the groupconsisting of hydrogen, OH, and halogen; R₆ and R₇ are eachindependently selected from the group consisting of hydrogen andhalogen; R₈ is selected from the group consisting of hydrogen, loweralkyl of from 1 to about 8 carbons, halogen, OCH₃, and CF₃; and R₁₃ isselected from the group consisting of hydrogen, lower alkyl of from 1 toabout 8 carbons, phenyl, halogen, OCH₃, CF₃, and —CH₂R′, wherein R′ ishalogen; wherein no more than one of R₁, R₂, and R₃ is OCH₃ or hydrogenand one, but not both, of R₄ and R₅ is OH; or a pharmaceuticallyacceptable salt thereof.
 11. The pharmaceutical composition of claim 10,wherein R₄ is OH and R₅ is hydrogen or halogen.
 12. The pharmaceuticalcomposition of claim 10, wherein R₅ is OH and R₄ is hydrogen or halogen.13. The pharmaceutical composition of claim 10, wherein R₆ and R₇ areeach halogen.
 14. The pharmaceutical composition of claim 10, wherein R₆and R₇ are each hydrogen.
 15. The pharmaceutical composition of claim10, wherein R₂ is OCH₃, NH₂, or NHCOR₁₃.
 16. The pharmaceuticalcomposition of claim 10, wherein R₁ and R₃ are halogen.
 17. Thepharmaceutical composition of claim 10, wherein R₁ is halogen, R₂ isOCH₃ or NH₂, and R₃ is hydrogen.
 18. The pharmaceutical composition ofclaim 10, wherein R₅ is OH, R₄ is hydrogen or halogen, R₂ is OCH₃, NH₂,or NHCOR₁₃, and R₁ and R₃ are halogen.
 19. A method of stimulating,regulating or modulating metabolism of fats in adipose tissue inanimals, comprising administering an effective amount of at least onecompound having the structure:

wherein: R₁ and R₃ are independently selected from the group consistingof hydrogen, halogen, alkyl, aryl alkyl, CF₃, and OCH₃; R₂ is selectedfrom the group consisting of hydrogen, halogen, OH, OCH₃, OCH₂COOH,C(O)-aryl, NCS, NH₂, N₃, NHR₈, NHCH₂COOH, NHCOR₁₃, NHCONHR₁₃, andNHCOSR₁₃; R₄ and R₅ are each independently selected from the groupconsisting of hydrogen, OH, and halogen; R₆ and R₇ are eachindependently selected from the group consisting of hydrogen andhalogen; R₈ is selected from the group consisting of hydrogen, loweralkyl of from 1 to about 8 carbons, halogen, OCH₃, and CF₃; and R₁₃ isselected from the group consisting of hydrogen, lower alkyl of from 1 toabout 8 carbons, phenyl, halogen, OCH₃, CF₃, and —CH₂R′, wherein R′ ishalogen; wherein no more than one of R₁, R₂, and R₃ is OCH₃ or hydrogenand one, but not both, of R₄ and R₅ is OH; or a pharmaceuticallyacceptable salt thereof.
 20. The method of claim 19, wherein R₄ is OHand R₅ is hydrogen or halogen.
 21. The method of claim 19, wherein R₅ isOH and R₄ is hydrogen or halogen.
 22. The method of claim 19, wherein R₆and R₇ are each halogen.
 23. The method of claim 19, wherein R₆ and R₇are each hydrogen.
 24. The method of claim 19, wherein R₂ is OCH₃, NH₂,or NHCOR₁₃.
 25. The method of claim 19, wherein R₁ and R₃ are halogen.26. The method of claim 19, wherein R₁ is halogen, R₂ is OCH₃ or NH₂,and R₃ is hydrogen.
 27. The method of claim 19, wherein the compound isadministered with at least one pharmaceutically acceptable carrier. 28.The method of claim 19, wherein R₅ is OH, R₄ is hydrogen or halogen, R₂is OCH₃, NH₂, or NHCOR₁₃, and R₁ and R₃ are halogen.